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What is the origin for RS553094345 SNP? | The origin is unknown. | <s>[INST] What is the origin for RS553094345 SNP? [/INST] The origin is unknown. </s> |
What is the type of genetic variation for RS553094345 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS553094345 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS553094345 SNP? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for RS553094345 SNP? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with RS1593539077 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593539077 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593539077 SNP. | <s>[INST] Which condition is asociated with RS1593539077 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593539077 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593539077 SNP. </s> |
In which chromosome is RS1593539077 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593539077 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593539077 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593539077 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593539077 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST] What is the clinical significance of RS1593539077 SNP, is it benign or pathogenic? [/INST] It is Benign. </s> |
How long is the variation length for RS1593539077 SNP? | The variation length is 8 base pairs. | <s>[INST] How long is the variation length for RS1593539077 SNP? [/INST] The variation length is 8 base pairs. </s> |
What is the origin for RS1593539077 SNP? | The origin is unknown. | <s>[INST] What is the origin for RS1593539077 SNP? [/INST] The origin is unknown. </s> |
What is the type of genetic variation for RS1593539077 SNP? | The variation is a Insertion. | <s>[INST] What is the type of genetic variation for RS1593539077 SNP? [/INST] The variation is a Insertion. </s> |
What is the genetic molecular consequence for RS1593539077 SNP? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for RS1593539077 SNP? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with RS1593539493 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593539493 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593539493 SNP. | <s>[INST] Which condition is asociated with RS1593539493 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593539493 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593539493 SNP. </s> |
In which chromosome is RS1593539493 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593539493 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593539493 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593539493 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593539493 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1593539493 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1593539493 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1593539493 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1593539493 SNP? | The origin is unknown. | <s>[INST] What is the origin for RS1593539493 SNP? [/INST] The origin is unknown. </s> |
What is the type of genetic variation for RS1593539493 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1593539493 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1593539493 SNP? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for RS1593539493 SNP? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with DUP820580? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDUP820580. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP820580. | <s>[INST] Which condition is asociated with DUP820580? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDUP820580. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP820580. </s> |
In which chromosome is DUP820580 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DUP820580 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DUP820580? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DUP820580? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DUP820580, is it benign or pathogenic? | It is Likely pathogenic. | <s>[INST] What is the clinical significance of DUP820580, is it benign or pathogenic? [/INST] It is Likely pathogenic. </s> |
How long is the variation length for DUP820580? | The variation length is 12396 base pairs. | <s>[INST] How long is the variation length for DUP820580? [/INST] The variation length is 12396 base pairs. </s> |
What is the origin for DUP820580? | The origin is germline. | <s>[INST] What is the origin for DUP820580? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DUP820580? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for DUP820580? [/INST] The variation is a Duplication. </s> |
Which condition is asociated with DEL820581? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDEL820581. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL820581. | <s>[INST] Which condition is asociated with DEL820581? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDEL820581. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL820581. </s> |
In which chromosome is DEL820581 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL820581 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL820581? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL820581? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL820581, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL820581, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL820581? | The variation length is 27099 base pairs. | <s>[INST] How long is the variation length for DEL820581? [/INST] The variation length is 27099 base pairs. </s> |
What is the origin for DEL820581? | The origin is germline. | <s>[INST] What is the origin for DEL820581? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL820581? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL820581? [/INST] The variation is a Deletion. </s> |
Which condition is asociated with DEL820572? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDEL820572. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL820572. | <s>[INST] Which condition is asociated with DEL820572? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDEL820572. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL820572. </s> |
In which chromosome is DEL820572 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL820572 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL820572? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL820572? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL820572, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL820572, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL820572? | The variation length is 359 base pairs. | <s>[INST] How long is the variation length for DEL820572? [/INST] The variation length is 359 base pairs. </s> |
What is the origin for DEL820572? | The origin is germline. | <s>[INST] What is the origin for DEL820572? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL820572? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL820572? [/INST] The variation is a Deletion. </s> |
Which condition is asociated with DEL820569? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDEL820569. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL820569. | <s>[INST] Which condition is asociated with DEL820569? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDEL820569. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL820569. </s> |
In which chromosome is DEL820569 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL820569 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL820569? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL820569? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL820569, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL820569, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL820569? | The variation length is 442325 base pairs. | <s>[INST] How long is the variation length for DEL820569? [/INST] The variation length is 442325 base pairs. </s> |
What is the origin for DEL820569? | The origin is germline. | <s>[INST] What is the origin for DEL820569? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL820569? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL820569? [/INST] The variation is a Deletion. </s> |
Which condition is asociated with DEL820571? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDEL820571. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL820571. | <s>[INST] Which condition is asociated with DEL820571? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDEL820571. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL820571. </s> |
In which chromosome is DEL820571 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL820571 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL820571? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL820571? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL820571, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL820571, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL820571? | The variation length is 180144 base pairs. | <s>[INST] How long is the variation length for DEL820571? [/INST] The variation length is 180144 base pairs. </s> |
What is the origin for DEL820571? | The origin is germline. | <s>[INST] What is the origin for DEL820571? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL820571? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL820571? [/INST] The variation is a Deletion. </s> |
Which condition is asociated with DUP820579? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDUP820579. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP820579. | <s>[INST] Which condition is asociated with DUP820579? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDUP820579. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP820579. </s> |
In which chromosome is DUP820579 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DUP820579 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DUP820579? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DUP820579? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DUP820579, is it benign or pathogenic? | It is Likely pathogenic. | <s>[INST] What is the clinical significance of DUP820579, is it benign or pathogenic? [/INST] It is Likely pathogenic. </s> |
How long is the variation length for DUP820579? | The variation length is 12400 base pairs. | <s>[INST] How long is the variation length for DUP820579? [/INST] The variation length is 12400 base pairs. </s> |
What is the origin for DUP820579? | The origin is germline. | <s>[INST] What is the origin for DUP820579? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DUP820579? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for DUP820579? [/INST] The variation is a Duplication. </s> |
Which condition is asociated with DEL820574? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDEL820574. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL820574. | <s>[INST] Which condition is asociated with DEL820574? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDEL820574. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL820574. </s> |
In which chromosome is DEL820574 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL820574 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL820574? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL820574? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL820574, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL820574, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL820574? | The variation length is 176371 base pairs. | <s>[INST] How long is the variation length for DEL820574? [/INST] The variation length is 176371 base pairs. </s> |
What is the origin for DEL820574? | The origin is germline. | <s>[INST] What is the origin for DEL820574? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL820574? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL820574? [/INST] The variation is a Deletion. </s> |
Which condition is asociated with DEL820573? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDEL820573. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL820573. | <s>[INST] Which condition is asociated with DEL820573? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDEL820573. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL820573. </s> |
In which chromosome is DEL820573 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL820573 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL820573? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL820573? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL820573, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL820573, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL820573? | The variation length is 109196 base pairs. | <s>[INST] How long is the variation length for DEL820573? [/INST] The variation length is 109196 base pairs. </s> |
What is the origin for DEL820573? | The origin is germline. | <s>[INST] What is the origin for DEL820573? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL820573? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL820573? [/INST] The variation is a Deletion. </s> |
Which condition is asociated with DEL820570? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDEL820570. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL820570. | <s>[INST] Which condition is asociated with DEL820570? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsDEL820570. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL820570. </s> |
In which chromosome is DEL820570 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL820570 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL820570? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL820570? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL820570, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL820570, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL820570? | The variation length is 439162 base pairs. | <s>[INST] How long is the variation length for DEL820570? [/INST] The variation length is 439162 base pairs. </s> |
What is the origin for DEL820570? | The origin is germline. | <s>[INST] What is the origin for DEL820570? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL820570? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL820570? [/INST] The variation is a Deletion. </s> |
Which condition is asociated with RS1949433098 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1949433098 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949433098 SNP. | <s>[INST] Which condition is asociated with RS1949433098 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1949433098 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949433098 SNP. </s> |
In which chromosome is RS1949433098 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1949433098 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1949433098 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1949433098 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1949433098 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1949433098 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1949433098 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1949433098 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1949433098 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1949433098 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1949433098 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS1949433098 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS1949433098 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS1949433098 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS1948522929 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1948522929 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1948522929 SNP. | <s>[INST] Which condition is asociated with RS1948522929 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1948522929 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1948522929 SNP. </s> |
In which chromosome is RS1948522929 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1948522929 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1948522929 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1948522929 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1948522929 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1948522929 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1948522929 SNP? | The variation length is 4 base pairs. | <s>[INST] How long is the variation length for RS1948522929 SNP? [/INST] The variation length is 4 base pairs. </s> |
What is the origin for RS1948522929 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1948522929 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1948522929 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS1948522929 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS1948522929 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS1948522929 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS1949505926 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1949505926 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949505926 SNP. | <s>[INST] Which condition is asociated with RS1949505926 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1949505926 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949505926 SNP. </s> |
In which chromosome is RS1949505926 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1949505926 SNP located? [/INST] It is located in the chromosome 13. </s> |