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What is the type of genetic variation for SNV1409060? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1409060? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1409060? | The resulting gene consequence is a splice acceptor variant. | <s>[INST] What is the genetic molecular consequence for SNV1409060? [/INST] The resulting gene consequence is a splice acceptor variant. </s> |
Which condition is asociated with SNV1415961? | 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/RsSNV1415961. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1415961. | <s>[INST] Which condition is asociated with SNV1415961? [/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/RsSNV1415961. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1415961. </s> |
In which chromosome is SNV1415961 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1415961 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1415961? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1415961? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1415961, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1415961, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1415961? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1415961? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1415961? | The origin is germline. | <s>[INST] What is the origin for SNV1415961? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1415961? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1415961? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1415961? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1415961? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV1484857? | 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/RsSNV1484857. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1484857. | <s>[INST] Which condition is asociated with SNV1484857? [/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/RsSNV1484857. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1484857. </s> |
In which chromosome is SNV1484857 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1484857 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1484857? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1484857? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1484857, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1484857, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1484857? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1484857? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1484857? | The origin is germline. | <s>[INST] What is the origin for SNV1484857? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1484857? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1484857? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1484857? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1484857? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV1400287? | 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/RsSNV1400287. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1400287. | <s>[INST] Which condition is asociated with SNV1400287? [/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/RsSNV1400287. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1400287. </s> |
In which chromosome is SNV1400287 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1400287 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1400287? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1400287? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1400287, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1400287, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1400287? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1400287? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1400287? | The origin is germline. | <s>[INST] What is the origin for SNV1400287? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1400287? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1400287? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1400287? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1400287? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV1428780? | 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/RsSNV1428780. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1428780. | <s>[INST] Which condition is asociated with SNV1428780? [/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/RsSNV1428780. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1428780. </s> |
In which chromosome is SNV1428780 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1428780 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1428780? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1428780? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1428780, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1428780, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1428780? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1428780? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1428780? | The origin is germline. | <s>[INST] What is the origin for SNV1428780? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1428780? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1428780? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1428780? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for SNV1428780? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with SNV1501129? | 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/RsSNV1501129. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1501129. | <s>[INST] Which condition is asociated with SNV1501129? [/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/RsSNV1501129. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1501129. </s> |
In which chromosome is SNV1501129 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1501129 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1501129? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1501129? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1501129, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1501129, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1501129? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1501129? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1501129? | The origin is germline. | <s>[INST] What is the origin for SNV1501129? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1501129? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1501129? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1501129? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1501129? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV1503449? | 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/RsSNV1503449. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1503449. | <s>[INST] Which condition is asociated with SNV1503449? [/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/RsSNV1503449. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1503449. </s> |
In which chromosome is SNV1503449 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1503449 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1503449? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1503449? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1503449, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1503449, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1503449? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1503449? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1503449? | The origin is germline. | <s>[INST] What is the origin for SNV1503449? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1503449? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1503449? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1503449? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1503449? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV1428784? | 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/RsSNV1428784. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1428784. | <s>[INST] Which condition is asociated with SNV1428784? [/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/RsSNV1428784. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1428784. </s> |
In which chromosome is SNV1428784 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1428784 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1428784? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1428784? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1428784, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1428784, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1428784? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1428784? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1428784? | The origin is germline. | <s>[INST] What is the origin for SNV1428784? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1428784? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1428784? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1428784? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1428784? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV1486041? | 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/RsSNV1486041. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1486041. | <s>[INST] Which condition is asociated with SNV1486041? [/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/RsSNV1486041. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1486041. </s> |
In which chromosome is SNV1486041 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1486041 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1486041? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1486041? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1486041, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1486041, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1486041? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1486041? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1486041? | The origin is germline. | <s>[INST] What is the origin for SNV1486041? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1486041? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1486041? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1486041? | The resulting gene consequence is a splice acceptor variant. | <s>[INST] What is the genetic molecular consequence for SNV1486041? [/INST] The resulting gene consequence is a splice acceptor variant. </s> |
Which condition is asociated with SNV1691189? | 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/RsSNV1691189. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1691189. | <s>[INST] Which condition is asociated with SNV1691189? [/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/RsSNV1691189. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1691189. </s> |
In which chromosome is SNV1691189 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1691189 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1691189? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1691189? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1691189, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1691189, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1691189? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1691189? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1691189? | The origin is germline. | <s>[INST] What is the origin for SNV1691189? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1691189? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1691189? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1691189? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1691189? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with RS1131690880 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/RsRS1131690880 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1131690880 SNP. | <s>[INST] Which condition is asociated with RS1131690880 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/RsRS1131690880 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1131690880 SNP. </s> |
In which chromosome is RS1131690880 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1131690880 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1131690880 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1131690880 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1131690880 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1131690880 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1131690880 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1131690880 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1131690880 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1131690880 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1131690880 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1131690880 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1131690880 SNP? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for RS1131690880 SNP? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with RS587776789 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/RsRS587776789 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587776789 SNP. | <s>[INST] Which condition is asociated with RS587776789 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/RsRS587776789 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587776789 SNP. </s> |
In which chromosome is RS587776789 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587776789 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587776789 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587776789 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587776789 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587776789 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587776789 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587776789 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587776789 SNP? | The origin is germline. | <s>[INST] What is the origin for RS587776789 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS587776789 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS587776789 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS587776789 SNP? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for RS587776789 SNP? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV1918434? | 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/RsSNV1918434. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1918434. | <s>[INST] Which condition is asociated with SNV1918434? [/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/RsSNV1918434. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1918434. </s> |
In which chromosome is SNV1918434 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1918434 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1918434? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1918434? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1918434, is it benign or pathogenic? | It is Likely pathogenic. | <s>[INST] What is the clinical significance of SNV1918434, is it benign or pathogenic? [/INST] It is Likely pathogenic. </s> |
How long is the variation length for SNV1918434? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1918434? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1918434? | The origin is germline. | <s>[INST] What is the origin for SNV1918434? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1918434? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1918434? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1918434? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1918434? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV2056034? | 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/RsSNV2056034. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV2056034. | <s>[INST] Which condition is asociated with SNV2056034? [/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/RsSNV2056034. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV2056034. </s> |
In which chromosome is SNV2056034 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV2056034 located? [/INST] It is located in the chromosome 13. </s> |