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What is the clinical significance of RS1593412272 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST] What is the clinical significance of RS1593412272 SNP, is it benign or pathogenic? [/INST] It is Uncertain significance. </s> |
How long is the variation length for RS1593412272 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1593412272 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1593412272 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1593412272 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1593412272 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1593412272 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1593412272 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS1593412272 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS1593532101 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/RsRS1593532101 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593532101 SNP. | <s>[INST] Which condition is asociated with RS1593532101 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/RsRS1593532101 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593532101 SNP. </s> |
In which chromosome is RS1593532101 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593532101 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593532101 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593532101 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593532101 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1593532101 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1593532101 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1593532101 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1593532101 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1593532101 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1593532101 SNP? | The variation is a Insertion. | <s>[INST] What is the type of genetic variation for RS1593532101 SNP? [/INST] The variation is a Insertion. </s> |
What is the genetic molecular consequence for RS1593532101 SNP? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for RS1593532101 SNP? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with DEL652514? | 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/RsDEL652514. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL652514. | <s>[INST] Which condition is asociated with DEL652514? [/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/RsDEL652514. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL652514. </s> |
In which chromosome is DEL652514 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL652514 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL652514? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL652514? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL652514, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL652514, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL652514? | The variation length is 3514 base pairs. | <s>[INST] How long is the variation length for DEL652514? [/INST] The variation length is 3514 base pairs. </s> |
What is the origin for DEL652514? | The origin is germline. | <s>[INST] What is the origin for DEL652514? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL652514? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL652514? [/INST] The variation is a Deletion. </s> |
Which condition is asociated with RS1593539538 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/RsRS1593539538 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593539538 SNP. | <s>[INST] Which condition is asociated with RS1593539538 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/RsRS1593539538 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593539538 SNP. </s> |
In which chromosome is RS1593539538 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593539538 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593539538 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593539538 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593539538 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1593539538 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1593539538 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1593539538 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1593539538 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1593539538 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1593539538 SNP? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for RS1593539538 SNP? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for RS1593539538 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS1593539538 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS1593457138 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/RsRS1593457138 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593457138 SNP. | <s>[INST] Which condition is asociated with RS1593457138 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/RsRS1593457138 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593457138 SNP. </s> |
In which chromosome is RS1593457138 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593457138 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593457138 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593457138 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593457138 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST] What is the clinical significance of RS1593457138 SNP, is it benign or pathogenic? [/INST] It is Uncertain significance. </s> |
How long is the variation length for RS1593457138 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1593457138 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1593457138 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1593457138 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1593457138 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1593457138 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1593457138 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS1593457138 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS1593529861 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/RsRS1593529861 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593529861 SNP. | <s>[INST] Which condition is asociated with RS1593529861 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/RsRS1593529861 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593529861 SNP. </s> |
In which chromosome is RS1593529861 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593529861 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593529861 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593529861 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593529861 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST] What is the clinical significance of RS1593529861 SNP, is it benign or pathogenic? [/INST] It is Uncertain significance. </s> |
How long is the variation length for RS1593529861 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1593529861 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1593529861 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1593529861 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1593529861 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1593529861 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1593529861 SNP? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for RS1593529861 SNP? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with DEL652281? | 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/RsDEL652281. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL652281. | <s>[INST] Which condition is asociated with DEL652281? [/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/RsDEL652281. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL652281. </s> |
In which chromosome is DEL652281 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL652281 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL652281? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL652281? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL652281, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL652281, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL652281? | The variation length is 41764 base pairs. | <s>[INST] How long is the variation length for DEL652281? [/INST] The variation length is 41764 base pairs. </s> |
What is the origin for DEL652281? | The origin is germline. | <s>[INST] What is the origin for DEL652281? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL652281? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL652281? [/INST] The variation is a Deletion. </s> |
Which condition is asociated with RS1593434175 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/RsRS1593434175 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593434175 SNP. | <s>[INST] Which condition is asociated with RS1593434175 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/RsRS1593434175 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593434175 SNP. </s> |
In which chromosome is RS1593434175 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593434175 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593434175 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593434175 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593434175 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1593434175 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1593434175 SNP? | The variation length is 5 base pairs. | <s>[INST] How long is the variation length for RS1593434175 SNP? [/INST] The variation length is 5 base pairs. </s> |
What is the origin for RS1593434175 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1593434175 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1593434175 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS1593434175 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS1593434175 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS1593434175 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS1593448511 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/RsRS1593448511 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593448511 SNP. | <s>[INST] Which condition is asociated with RS1593448511 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/RsRS1593448511 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593448511 SNP. </s> |
In which chromosome is RS1593448511 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593448511 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593448511 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593448511 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593448511 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST] What is the clinical significance of RS1593448511 SNP, is it benign or pathogenic? [/INST] It is Uncertain significance. </s> |
How long is the variation length for RS1593448511 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1593448511 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1593448511 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1593448511 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1593448511 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1593448511 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1593448511 SNP? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for RS1593448511 SNP? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with RS1593454115 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/RsRS1593454115 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593454115 SNP. | <s>[INST] Which condition is asociated with RS1593454115 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/RsRS1593454115 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593454115 SNP. </s> |
In which chromosome is RS1593454115 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593454115 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593454115 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593454115 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593454115 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1593454115 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1593454115 SNP? | The variation length is 2 base pairs. | <s>[INST] How long is the variation length for RS1593454115 SNP? [/INST] The variation length is 2 base pairs. </s> |
What is the origin for RS1593454115 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1593454115 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1593454115 SNP? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for RS1593454115 SNP? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for RS1593454115 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS1593454115 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS1593411974 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/RsRS1593411974 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593411974 SNP. | <s>[INST] Which condition is asociated with RS1593411974 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/RsRS1593411974 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593411974 SNP. </s> |
In which chromosome is RS1593411974 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593411974 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593411974 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593411974 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593411974 SNP, is it benign or pathogenic? | It is Likely pathogenic. | <s>[INST] What is the clinical significance of RS1593411974 SNP, is it benign or pathogenic? [/INST] It is Likely pathogenic. </s> |
How long is the variation length for RS1593411974 SNP? | The variation length is 32 base pairs. | <s>[INST] How long is the variation length for RS1593411974 SNP? [/INST] The variation length is 32 base pairs. </s> |
What is the origin for RS1593411974 SNP? | The origin is unknown. | <s>[INST] What is the origin for RS1593411974 SNP? [/INST] The origin is unknown. </s> |
What is the type of genetic variation for RS1593411974 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS1593411974 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS1593411974 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS1593411974 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS1312883856 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/RsRS1312883856 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1312883856 SNP. | <s>[INST] Which condition is asociated with RS1312883856 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/RsRS1312883856 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1312883856 SNP. </s> |
In which chromosome is RS1312883856 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1312883856 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1312883856 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1312883856 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1312883856 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST] What is the clinical significance of RS1312883856 SNP, is it benign or pathogenic? [/INST] It is Uncertain significance. </s> |
How long is the variation length for RS1312883856 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1312883856 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1312883856 SNP? | The origin is unknown. | <s>[INST] What is the origin for RS1312883856 SNP? [/INST] The origin is unknown. </s> |
What is the type of genetic variation for RS1312883856 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1312883856 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1312883856 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS1312883856 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS1593443469 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/RsRS1593443469 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593443469 SNP. | <s>[INST] Which condition is asociated with RS1593443469 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/RsRS1593443469 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593443469 SNP. </s> |
In which chromosome is RS1593443469 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593443469 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593443469 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593443469 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593443469 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST] What is the clinical significance of RS1593443469 SNP, is it benign or pathogenic? [/INST] It is Uncertain significance. </s> |
How long is the variation length for RS1593443469 SNP? | The variation length is 6 base pairs. | <s>[INST] How long is the variation length for RS1593443469 SNP? [/INST] The variation length is 6 base pairs. </s> |
What is the origin for RS1593443469 SNP? | The origin is unknown. | <s>[INST] What is the origin for RS1593443469 SNP? [/INST] The origin is unknown. </s> |
What is the type of genetic variation for RS1593443469 SNP? | The variation is a Insertion. | <s>[INST] What is the type of genetic variation for RS1593443469 SNP? [/INST] The variation is a Insertion. </s> |
What is the genetic molecular consequence for RS1593443469 SNP? | The resulting gene consequence is a inframe_indel. | <s>[INST] What is the genetic molecular consequence for RS1593443469 SNP? [/INST] The resulting gene consequence is a inframe_indel. </s> |
Which condition is asociated with RS1593443514 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/RsRS1593443514 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593443514 SNP. | <s>[INST] Which condition is asociated with RS1593443514 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/RsRS1593443514 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593443514 SNP. </s> |