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What is the clinical significance of RS587778862 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778862 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778862 SNP? | The variation length is 2 base pairs. | <s>[INST] How long is the variation length for RS587778862 SNP? [/INST] The variation length is 2 base pairs. </s> |
What is the origin for RS587778862 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778862 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778862 SNP? | The variation is a Microsatellite. | <s>[INST] What is the type of genetic variation for RS587778862 SNP? [/INST] The variation is a Microsatellite. </s> |
What is the genetic molecular consequence for RS587778862 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587778862 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS587778824 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/RsRS587778824 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778824 SNP. | <s>[INST] Which condition is asociated with RS587778824 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/RsRS587778824 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778824 SNP. </s> |
In which chromosome is RS587778824 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778824 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778824 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778824 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778824 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778824 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778824 SNP? | The variation length is 2 base pairs. | <s>[INST] How long is the variation length for RS587778824 SNP? [/INST] The variation length is 2 base pairs. </s> |
What is the origin for RS587778824 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778824 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778824 SNP? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for RS587778824 SNP? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for RS587778824 SNP? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for RS587778824 SNP? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with RS145310579 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/RsRS145310579 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS145310579 SNP. | <s>[INST] Which condition is asociated with RS145310579 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/RsRS145310579 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS145310579 SNP. </s> |
In which chromosome is RS145310579 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS145310579 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS145310579 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS145310579 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS145310579 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST] What is the clinical significance of RS145310579 SNP, is it benign or pathogenic? [/INST] It is Benign. </s> |
How long is the variation length for RS145310579 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS145310579 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS145310579 SNP? | The origin is germline. | <s>[INST] What is the origin for RS145310579 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS145310579 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS145310579 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS145310579 SNP? | The resulting gene consequence is a synonymous variant. | <s>[INST] What is the genetic molecular consequence for RS145310579 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s> |
Which condition is asociated with RS187110786 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/RsRS187110786 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS187110786 SNP. | <s>[INST] Which condition is asociated with RS187110786 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/RsRS187110786 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS187110786 SNP. </s> |
In which chromosome is RS187110786 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS187110786 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS187110786 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS187110786 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS187110786 SNP, is it benign or pathogenic? | It is Benign/Likely benign. | <s>[INST] What is the clinical significance of RS187110786 SNP, is it benign or pathogenic? [/INST] It is Benign/Likely benign. </s> |
How long is the variation length for RS187110786 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS187110786 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS187110786 SNP? | The origin is germline. | <s>[INST] What is the origin for RS187110786 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS187110786 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS187110786 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS187110786 SNP? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for RS187110786 SNP? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with RS572454921 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/RsRS572454921 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS572454921 SNP. | <s>[INST] Which condition is asociated with RS572454921 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/RsRS572454921 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS572454921 SNP. </s> |
In which chromosome is RS572454921 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS572454921 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS572454921 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS572454921 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS572454921 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST] What is the clinical significance of RS572454921 SNP, is it benign or pathogenic? [/INST] It is Benign. </s> |
How long is the variation length for RS572454921 SNP? | The variation length is 9 base pairs. | <s>[INST] How long is the variation length for RS572454921 SNP? [/INST] The variation length is 9 base pairs. </s> |
What is the origin for RS572454921 SNP? | The origin is germline. | <s>[INST] What is the origin for RS572454921 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS572454921 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS572454921 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS572454921 SNP? | The resulting gene consequence is a inframe_deletion. | <s>[INST] What is the genetic molecular consequence for RS572454921 SNP? [/INST] The resulting gene consequence is a inframe_deletion. </s> |
Which condition is asociated with RS4151624 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/RsRS4151624 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS4151624 SNP. | <s>[INST] Which condition is asociated with RS4151624 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/RsRS4151624 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS4151624 SNP. </s> |
In which chromosome is RS4151624 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS4151624 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS4151624 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS4151624 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS4151624 SNP, is it benign or pathogenic? | It is Benign/Likely benign. | <s>[INST] What is the clinical significance of RS4151624 SNP, is it benign or pathogenic? [/INST] It is Benign/Likely benign. </s> |
How long is the variation length for RS4151624 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS4151624 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS4151624 SNP? | The origin is unknown. | <s>[INST] What is the origin for RS4151624 SNP? [/INST] The origin is unknown. </s> |
What is the type of genetic variation for RS4151624 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS4151624 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS4151624 SNP? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for RS4151624 SNP? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with RS9535023 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/RsRS9535023 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS9535023 SNP. | <s>[INST] Which condition is asociated with RS9535023 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/RsRS9535023 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS9535023 SNP. </s> |
In which chromosome is RS9535023 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS9535023 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS9535023 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS9535023 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS9535023 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST] What is the clinical significance of RS9535023 SNP, is it benign or pathogenic? [/INST] It is Benign. </s> |
How long is the variation length for RS9535023 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS9535023 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS9535023 SNP? | The origin is germline. | <s>[INST] What is the origin for RS9535023 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS9535023 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS9535023 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS9535023 SNP? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for RS9535023 SNP? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with RS753117180 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/RsRS753117180 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS753117180 SNP. | <s>[INST] Which condition is asociated with RS753117180 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/RsRS753117180 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS753117180 SNP. </s> |
In which chromosome is RS753117180 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS753117180 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS753117180 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS753117180 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS753117180 SNP, is it benign or pathogenic? | It is Conflicting interpretations of pathogenicity. | <s>[INST] What is the clinical significance of RS753117180 SNP, is it benign or pathogenic? [/INST] It is Conflicting interpretations of pathogenicity. </s> |
How long is the variation length for RS753117180 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS753117180 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS753117180 SNP? | The origin is germline. | <s>[INST] What is the origin for RS753117180 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS753117180 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS753117180 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS753117180 SNP? | The resulting gene consequence is a 5 prime UTR variant. | <s>[INST] What is the genetic molecular consequence for RS753117180 SNP? [/INST] The resulting gene consequence is a 5 prime UTR variant. </s> |
Which condition is asociated with RS375751988 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/RsRS375751988 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS375751988 SNP. | <s>[INST] Which condition is asociated with RS375751988 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/RsRS375751988 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS375751988 SNP. </s> |
In which chromosome is RS375751988 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS375751988 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS375751988 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS375751988 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS375751988 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST] What is the clinical significance of RS375751988 SNP, is it benign or pathogenic? [/INST] It is Benign. </s> |
How long is the variation length for RS375751988 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS375751988 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS375751988 SNP? | The origin is germline. | <s>[INST] What is the origin for RS375751988 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS375751988 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS375751988 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS375751988 SNP? | The resulting gene consequence is a synonymous variant. | <s>[INST] What is the genetic molecular consequence for RS375751988 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s> |
Which condition is asociated with RS587778823 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/RsRS587778823 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778823 SNP. | <s>[INST] Which condition is asociated with RS587778823 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/RsRS587778823 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778823 SNP. </s> |
In which chromosome is RS587778823 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778823 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778823 SNP? | Associated methods are: research, clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778823 SNP? [/INST] Associated methods are: research, clinical testing. </s> |
What is the clinical significance of RS587778823 SNP, is it benign or pathogenic? | It is Likely benign. | <s>[INST] What is the clinical significance of RS587778823 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s> |
How long is the variation length for RS587778823 SNP? | The variation length is 3 base pairs. | <s>[INST] How long is the variation length for RS587778823 SNP? [/INST] The variation length is 3 base pairs. </s> |
What is the origin for RS587778823 SNP? | The origin is germline. | <s>[INST] What is the origin for RS587778823 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS587778823 SNP? | The variation is a Microsatellite. | <s>[INST] What is the type of genetic variation for RS587778823 SNP? [/INST] The variation is a Microsatellite. </s> |
What is the genetic molecular consequence for RS587778823 SNP? | The resulting gene consequence is a inframe_deletion. | <s>[INST] What is the genetic molecular consequence for RS587778823 SNP? [/INST] The resulting gene consequence is a inframe_deletion. </s> |
Which condition is asociated with RS150115447 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/RsRS150115447 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS150115447 SNP. | <s>[INST] Which condition is asociated with RS150115447 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/RsRS150115447 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS150115447 SNP. </s> |
In which chromosome is RS150115447 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS150115447 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS150115447 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS150115447 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS150115447 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST] What is the clinical significance of RS150115447 SNP, is it benign or pathogenic? [/INST] It is Benign. </s> |
How long is the variation length for RS150115447 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS150115447 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS150115447 SNP? | The origin is germline. | <s>[INST] What is the origin for RS150115447 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS150115447 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS150115447 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS150115447 SNP? | The resulting gene consequence is a synonymous variant. | <s>[INST] What is the genetic molecular consequence for RS150115447 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s> |
Which condition is asociated with RS864622373 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/RsRS864622373 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS864622373 SNP. | <s>[INST] Which condition is asociated with RS864622373 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/RsRS864622373 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS864622373 SNP. </s> |
In which chromosome is RS864622373 SNP located? | It is located in the chromosome 17. | <s>[INST] In which chromosome is RS864622373 SNP located? [/INST] It is located in the chromosome 17. </s> |
Which methods support the evidence found for the RS864622373 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS864622373 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS864622373 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST] What is the clinical significance of RS864622373 SNP, is it benign or pathogenic? [/INST] It is Uncertain significance. </s> |
How long is the variation length for RS864622373 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS864622373 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS864622373 SNP? | The origin is germline. | <s>[INST] What is the origin for RS864622373 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS864622373 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS864622373 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS864622373 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS864622373 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS143105337 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/RsRS143105337 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS143105337 SNP. | <s>[INST] Which condition is asociated with RS143105337 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/RsRS143105337 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS143105337 SNP. </s> |
In which chromosome is RS143105337 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS143105337 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS143105337 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS143105337 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS143105337 SNP, is it benign or pathogenic? | It is Likely benign. | <s>[INST] What is the clinical significance of RS143105337 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s> |
How long is the variation length for RS143105337 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS143105337 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS143105337 SNP? | The origin is germline. | <s>[INST] What is the origin for RS143105337 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS143105337 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS143105337 SNP? [/INST] The variation is a single nucleotide variant. </s> |