Datasets:

abirT

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combined_ophthalmology_validation_dataset

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In which chromosome is RS1593443514 SNP located?

It is located in the chromosome 13.

<s>[INST] In which chromosome is RS1593443514 SNP located? [/INST] It is located in the chromosome 13. </s>

Which methods support the evidence found for the RS1593443514 SNP?

Associated methods are: clinical testing.

<s>[INST] Which methods support the evidence found for the RS1593443514 SNP? [/INST] Associated methods are: clinical testing. </s>

What is the clinical significance of RS1593443514 SNP, is it benign or pathogenic?

It is Pathogenic.

<s>[INST] What is the clinical significance of RS1593443514 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s>

How long is the variation length for RS1593443514 SNP?

The variation length is 1 base pairs.

<s>[INST] How long is the variation length for RS1593443514 SNP? [/INST] The variation length is 1 base pairs. </s>

What is the origin for RS1593443514 SNP?

The origin is unknown.

<s>[INST] What is the origin for RS1593443514 SNP? [/INST] The origin is unknown. </s>

What is the type of genetic variation for RS1593443514 SNP?

The variation is a Deletion.

<s>[INST] What is the type of genetic variation for RS1593443514 SNP? [/INST] The variation is a Deletion. </s>

What is the genetic molecular consequence for RS1593443514 SNP?

The resulting gene consequence is a frameshift variant.

<s>[INST] What is the genetic molecular consequence for RS1593443514 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s>

Which condition is asociated with RS1285629437 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/RsRS1285629437 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1285629437 SNP.

<s>[INST] Which condition is asociated with RS1285629437 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/RsRS1285629437 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1285629437 SNP. </s>

In which chromosome is RS1285629437 SNP located?

It is located in the chromosome 13.

<s>[INST] In which chromosome is RS1285629437 SNP located? [/INST] It is located in the chromosome 13. </s>

Which methods support the evidence found for the RS1285629437 SNP?

Associated methods are: clinical testing.

<s>[INST] Which methods support the evidence found for the RS1285629437 SNP? [/INST] Associated methods are: clinical testing. </s>

What is the clinical significance of RS1285629437 SNP, is it benign or pathogenic?

It is Benign.

<s>[INST] What is the clinical significance of RS1285629437 SNP, is it benign or pathogenic? [/INST] It is Benign. </s>

How long is the variation length for RS1285629437 SNP?

The variation length is 1 base pairs.

<s>[INST] How long is the variation length for RS1285629437 SNP? [/INST] The variation length is 1 base pairs. </s>

What is the origin for RS1285629437 SNP?

The origin is unknown.

<s>[INST] What is the origin for RS1285629437 SNP? [/INST] The origin is unknown. </s>

What is the type of genetic variation for RS1285629437 SNP?

The variation is a single nucleotide variant.

<s>[INST] What is the type of genetic variation for RS1285629437 SNP? [/INST] The variation is a single nucleotide variant. </s>

What is the genetic molecular consequence for RS1285629437 SNP?

The resulting gene consequence is a intron variant.

<s>[INST] What is the genetic molecular consequence for RS1285629437 SNP? [/INST] The resulting gene consequence is a intron variant. </s>

Which condition is asociated with RS955333850 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/RsRS955333850 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS955333850 SNP.

<s>[INST] Which condition is asociated with RS955333850 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/RsRS955333850 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS955333850 SNP. </s>

In which chromosome is RS955333850 SNP located?

It is located in the chromosome 13.

<s>[INST] In which chromosome is RS955333850 SNP located? [/INST] It is located in the chromosome 13. </s>

Which methods support the evidence found for the RS955333850 SNP?

Associated methods are: clinical testing.

<s>[INST] Which methods support the evidence found for the RS955333850 SNP? [/INST] Associated methods are: clinical testing. </s>

What is the clinical significance of RS955333850 SNP, is it benign or pathogenic?

It is Benign.

<s>[INST] What is the clinical significance of RS955333850 SNP, is it benign or pathogenic? [/INST] It is Benign. </s>

How long is the variation length for RS955333850 SNP?

The variation length is 1 base pairs.

<s>[INST] How long is the variation length for RS955333850 SNP? [/INST] The variation length is 1 base pairs. </s>

What is the origin for RS955333850 SNP?

The origin is unknown.

<s>[INST] What is the origin for RS955333850 SNP? [/INST] The origin is unknown. </s>

What is the type of genetic variation for RS955333850 SNP?

The variation is a single nucleotide variant.

<s>[INST] What is the type of genetic variation for RS955333850 SNP? [/INST] The variation is a single nucleotide variant. </s>

What is the genetic molecular consequence for RS955333850 SNP?

The resulting gene consequence is a intron variant.

<s>[INST] What is the genetic molecular consequence for RS955333850 SNP? [/INST] The resulting gene consequence is a intron variant. </s>

Which condition is asociated with RS749894411 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/RsRS749894411 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS749894411 SNP.

<s>[INST] Which condition is asociated with RS749894411 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/RsRS749894411 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS749894411 SNP. </s>

In which chromosome is RS749894411 SNP located?

It is located in the chromosome 13.

<s>[INST] In which chromosome is RS749894411 SNP located? [/INST] It is located in the chromosome 13. </s>

Which methods support the evidence found for the RS749894411 SNP?

Associated methods are: clinical testing.

<s>[INST] Which methods support the evidence found for the RS749894411 SNP? [/INST] Associated methods are: clinical testing. </s>

What is the clinical significance of RS749894411 SNP, is it benign or pathogenic?

It is Likely benign.

<s>[INST] What is the clinical significance of RS749894411 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>

How long is the variation length for RS749894411 SNP?

The variation length is 1 base pairs.

<s>[INST] How long is the variation length for RS749894411 SNP? [/INST] The variation length is 1 base pairs. </s>

What is the origin for RS749894411 SNP?

The origin is unknown.

<s>[INST] What is the origin for RS749894411 SNP? [/INST] The origin is unknown. </s>

What is the type of genetic variation for RS749894411 SNP?

The variation is a single nucleotide variant.

<s>[INST] What is the type of genetic variation for RS749894411 SNP? [/INST] The variation is a single nucleotide variant. </s>

What is the genetic molecular consequence for RS749894411 SNP?

The resulting gene consequence is a intron variant.

<s>[INST] What is the genetic molecular consequence for RS749894411 SNP? [/INST] The resulting gene consequence is a intron variant. </s>

Which condition is asociated with RS1177544722 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/RsRS1177544722 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1177544722 SNP.

<s>[INST] Which condition is asociated with RS1177544722 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/RsRS1177544722 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1177544722 SNP. </s>

In which chromosome is RS1177544722 SNP located?

It is located in the chromosome 13.

<s>[INST] In which chromosome is RS1177544722 SNP located? [/INST] It is located in the chromosome 13. </s>

Which methods support the evidence found for the RS1177544722 SNP?

Associated methods are: clinical testing.

<s>[INST] Which methods support the evidence found for the RS1177544722 SNP? [/INST] Associated methods are: clinical testing. </s>

What is the clinical significance of RS1177544722 SNP, is it benign or pathogenic?

It is Likely benign.

<s>[INST] What is the clinical significance of RS1177544722 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>

How long is the variation length for RS1177544722 SNP?

The variation length is 2 base pairs.

<s>[INST] How long is the variation length for RS1177544722 SNP? [/INST] The variation length is 2 base pairs. </s>

What is the origin for RS1177544722 SNP?

The origin is unknown.

<s>[INST] What is the origin for RS1177544722 SNP? [/INST] The origin is unknown. </s>

What is the type of genetic variation for RS1177544722 SNP?

The variation is a Deletion.

<s>[INST] What is the type of genetic variation for RS1177544722 SNP? [/INST] The variation is a Deletion. </s>

What is the genetic molecular consequence for RS1177544722 SNP?

The resulting gene consequence is a frameshift variant.

<s>[INST] What is the genetic molecular consequence for RS1177544722 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s>

Which condition is asociated with RS1370123231 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/RsRS1370123231 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1370123231 SNP.

<s>[INST] Which condition is asociated with RS1370123231 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/RsRS1370123231 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1370123231 SNP. </s>

In which chromosome is RS1370123231 SNP located?

It is located in the chromosome 13.

<s>[INST] In which chromosome is RS1370123231 SNP located? [/INST] It is located in the chromosome 13. </s>

Which methods support the evidence found for the RS1370123231 SNP?

Associated methods are: clinical testing.

<s>[INST] Which methods support the evidence found for the RS1370123231 SNP? [/INST] Associated methods are: clinical testing. </s>

What is the clinical significance of RS1370123231 SNP, is it benign or pathogenic?

It is Uncertain significance.

<s>[INST] What is the clinical significance of RS1370123231 SNP, is it benign or pathogenic? [/INST] It is Uncertain significance. </s>

How long is the variation length for RS1370123231 SNP?

The variation length is 8 base pairs.

<s>[INST] How long is the variation length for RS1370123231 SNP? [/INST] The variation length is 8 base pairs. </s>

What is the origin for RS1370123231 SNP?

The origin is unknown.

<s>[INST] What is the origin for RS1370123231 SNP? [/INST] The origin is unknown. </s>

What is the type of genetic variation for RS1370123231 SNP?

The variation is a Insertion.

<s>[INST] What is the type of genetic variation for RS1370123231 SNP? [/INST] The variation is a Insertion. </s>

What is the genetic molecular consequence for RS1370123231 SNP?

The resulting gene consequence is a frameshift variant.

<s>[INST] What is the genetic molecular consequence for RS1370123231 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s>

Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP.

<s>[INST] Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP. </s>

In which chromosome is RS553094345 SNP located?

It is located in the chromosome 13.

<s>[INST] In which chromosome is RS553094345 SNP located? [/INST] It is located in the chromosome 13. </s>

Which methods support the evidence found for the RS553094345 SNP?

Associated methods are: clinical testing.

<s>[INST] Which methods support the evidence found for the RS553094345 SNP? [/INST] Associated methods are: clinical testing. </s>

What is the clinical significance of RS553094345 SNP, is it benign or pathogenic?

It is Benign.

<s>[INST] What is the clinical significance of RS553094345 SNP, is it benign or pathogenic? [/INST] It is Benign. </s>

How long is the variation length for RS553094345 SNP?

The variation length is 1 base pairs.

<s>[INST] How long is the variation length for RS553094345 SNP? [/INST] The variation length is 1 base pairs. </s>

What is the origin for RS553094345 SNP?

The origin is unknown.

<s>[INST] What is the origin for RS553094345 SNP? [/INST] The origin is unknown. </s>

What is the type of genetic variation for RS553094345 SNP?

The variation is a Duplication.

<s>[INST] What is the type of genetic variation for RS553094345 SNP? [/INST] The variation is a Duplication. </s>

What is the genetic molecular consequence for RS553094345 SNP?

The resulting gene consequence is a intron variant.

<s>[INST] What is the genetic molecular consequence for RS553094345 SNP? [/INST] The resulting gene consequence is a intron variant. </s>

Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP.

<s>[INST] Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP. </s>

In which chromosome is RS553094345 SNP located?

It is located in the chromosome 13.

<s>[INST] In which chromosome is RS553094345 SNP located? [/INST] It is located in the chromosome 13. </s>

Which methods support the evidence found for the RS553094345 SNP?

Associated methods are: clinical testing.

<s>[INST] Which methods support the evidence found for the RS553094345 SNP? [/INST] Associated methods are: clinical testing. </s>

What is the clinical significance of RS553094345 SNP, is it benign or pathogenic?

It is Benign.

<s>[INST] What is the clinical significance of RS553094345 SNP, is it benign or pathogenic? [/INST] It is Benign. </s>

How long is the variation length for RS553094345 SNP?

The variation length is 2 base pairs.

<s>[INST] How long is the variation length for RS553094345 SNP? [/INST] The variation length is 2 base pairs. </s>

What is the origin for RS553094345 SNP?

The origin is unknown.

<s>[INST] What is the origin for RS553094345 SNP? [/INST] The origin is unknown. </s>

What is the type of genetic variation for RS553094345 SNP?

The variation is a Duplication.

<s>[INST] What is the type of genetic variation for RS553094345 SNP? [/INST] The variation is a Duplication. </s>

What is the genetic molecular consequence for RS553094345 SNP?

The resulting gene consequence is a intron variant.

<s>[INST] What is the genetic molecular consequence for RS553094345 SNP? [/INST] The resulting gene consequence is a intron variant. </s>

Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP.

<s>[INST] Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP. </s>

In which chromosome is RS553094345 SNP located?

It is located in the chromosome 13.

<s>[INST] In which chromosome is RS553094345 SNP located? [/INST] It is located in the chromosome 13. </s>

Which methods support the evidence found for the RS553094345 SNP?

Associated methods are: clinical testing.

<s>[INST] Which methods support the evidence found for the RS553094345 SNP? [/INST] Associated methods are: clinical testing. </s>

What is the clinical significance of RS553094345 SNP, is it benign or pathogenic?

It is Benign.

<s>[INST] What is the clinical significance of RS553094345 SNP, is it benign or pathogenic? [/INST] It is Benign. </s>

How long is the variation length for RS553094345 SNP?

The variation length is 3 base pairs.

<s>[INST] How long is the variation length for RS553094345 SNP? [/INST] The variation length is 3 base pairs. </s>

What is the origin for RS553094345 SNP?

The origin is unknown.

<s>[INST] What is the origin for RS553094345 SNP? [/INST] The origin is unknown. </s>

What is the type of genetic variation for RS553094345 SNP?

The variation is a Duplication.

<s>[INST] What is the type of genetic variation for RS553094345 SNP? [/INST] The variation is a Duplication. </s>

What is the genetic molecular consequence for RS553094345 SNP?

The resulting gene consequence is a intron variant.

<s>[INST] What is the genetic molecular consequence for RS553094345 SNP? [/INST] The resulting gene consequence is a intron variant. </s>

Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP.

<s>[INST] Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP. </s>

In which chromosome is RS553094345 SNP located?

It is located in the chromosome 13.

<s>[INST] In which chromosome is RS553094345 SNP located? [/INST] It is located in the chromosome 13. </s>

Which methods support the evidence found for the RS553094345 SNP?

Associated methods are: clinical testing.

<s>[INST] Which methods support the evidence found for the RS553094345 SNP? [/INST] Associated methods are: clinical testing. </s>

What is the clinical significance of RS553094345 SNP, is it benign or pathogenic?

It is Benign.

<s>[INST] What is the clinical significance of RS553094345 SNP, is it benign or pathogenic? [/INST] It is Benign. </s>

How long is the variation length for RS553094345 SNP?

The variation length is 14 base pairs.

<s>[INST] How long is the variation length for RS553094345 SNP? [/INST] The variation length is 14 base pairs. </s>

What is the origin for RS553094345 SNP?

The origin is unknown.

<s>[INST] What is the origin for RS553094345 SNP? [/INST] The origin is unknown. </s>

What is the type of genetic variation for RS553094345 SNP?

The variation is a Duplication.

<s>[INST] What is the type of genetic variation for RS553094345 SNP? [/INST] The variation is a Duplication. </s>

What is the genetic molecular consequence for RS553094345 SNP?

The resulting gene consequence is a intron variant.

<s>[INST] What is the genetic molecular consequence for RS553094345 SNP? [/INST] The resulting gene consequence is a intron variant. </s>

Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP.

<s>[INST] Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP. </s>

In which chromosome is RS553094345 SNP located?

It is located in the chromosome 13.

<s>[INST] In which chromosome is RS553094345 SNP located? [/INST] It is located in the chromosome 13. </s>

Which methods support the evidence found for the RS553094345 SNP?

Associated methods are: clinical testing.

<s>[INST] Which methods support the evidence found for the RS553094345 SNP? [/INST] Associated methods are: clinical testing. </s>

What is the clinical significance of RS553094345 SNP, is it benign or pathogenic?

It is Benign.

<s>[INST] What is the clinical significance of RS553094345 SNP, is it benign or pathogenic? [/INST] It is Benign. </s>

How long is the variation length for RS553094345 SNP?

The variation length is 22 base pairs.

<s>[INST] How long is the variation length for RS553094345 SNP? [/INST] The variation length is 22 base pairs. </s>

What is the origin for RS553094345 SNP?

The origin is unknown.

<s>[INST] What is the origin for RS553094345 SNP? [/INST] The origin is unknown. </s>

What is the type of genetic variation for RS553094345 SNP?

The variation is a Duplication.

<s>[INST] What is the type of genetic variation for RS553094345 SNP? [/INST] The variation is a Duplication. </s>

What is the genetic molecular consequence for RS553094345 SNP?

The resulting gene consequence is a intron variant.

<s>[INST] What is the genetic molecular consequence for RS553094345 SNP? [/INST] The resulting gene consequence is a intron variant. </s>

Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP.

<s>[INST] Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP. </s>

In which chromosome is RS553094345 SNP located?

It is located in the chromosome 13.

<s>[INST] In which chromosome is RS553094345 SNP located? [/INST] It is located in the chromosome 13. </s>

Which methods support the evidence found for the RS553094345 SNP?

Associated methods are: clinical testing.

<s>[INST] Which methods support the evidence found for the RS553094345 SNP? [/INST] Associated methods are: clinical testing. </s>

What is the clinical significance of RS553094345 SNP, is it benign or pathogenic?

It is Benign.

<s>[INST] What is the clinical significance of RS553094345 SNP, is it benign or pathogenic? [/INST] It is Benign. </s>

How long is the variation length for RS553094345 SNP?

The variation length is 2 base pairs.

<s>[INST] How long is the variation length for RS553094345 SNP? [/INST] The variation length is 2 base pairs. </s>

What is the origin for RS553094345 SNP?

The origin is unknown.

<s>[INST] What is the origin for RS553094345 SNP? [/INST] The origin is unknown. </s>

What is the type of genetic variation for RS553094345 SNP?

The variation is a Deletion.

<s>[INST] What is the type of genetic variation for RS553094345 SNP? [/INST] The variation is a Deletion. </s>

What is the genetic molecular consequence for RS553094345 SNP?

The resulting gene consequence is a intron variant.

<s>[INST] What is the genetic molecular consequence for RS553094345 SNP? [/INST] The resulting gene consequence is a intron variant. </s>

Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP.

<s>[INST] Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP. </s>

In which chromosome is RS553094345 SNP located?

It is located in the chromosome 13.

<s>[INST] In which chromosome is RS553094345 SNP located? [/INST] It is located in the chromosome 13. </s>

Which methods support the evidence found for the RS553094345 SNP?

Associated methods are: clinical testing.

<s>[INST] Which methods support the evidence found for the RS553094345 SNP? [/INST] Associated methods are: clinical testing. </s>

What is the clinical significance of RS553094345 SNP, is it benign or pathogenic?

It is Benign.

<s>[INST] What is the clinical significance of RS553094345 SNP, is it benign or pathogenic? [/INST] It is Benign. </s>

How long is the variation length for RS553094345 SNP?

The variation length is 3 base pairs.

<s>[INST] How long is the variation length for RS553094345 SNP? [/INST] The variation length is 3 base pairs. </s>