rs10492519
A SNP in the FAM124A gene on chromosome 13. Its most notable genotype is G;G: Increased risk of developing prostate cancer
- Gene
- FAM124A
- Location
- Chr 1351,250,192 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 21%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AGoodNormal risk of developing prostate cancer
- A;GBadSlightly increased risk of developing prostate cancer
- G;GMost notableBadIncreased risk of developing prostate cancer
On SNPedia: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageA;A 76% A;G 19% G;G 5%
- European ancestry (Utah)A;A 29% A;G 46% G;G 25%
- Han Chinese (Beijing)A;A 96% A;G 4% G;G 0%
- Japanese (Tokyo)A;A 97% A;G 4% G;G 0%
- Yoruba (Nigeria)A;A 100% A;G 0% G;G 0%
- African ancestry (Southwest US)A;A 93% A;G 7% G;G 0%
- Chinese (Denver)A;A 99% A;G <1% G;G 0%
- Gujarati IndianA;A 52% A;G 44% G;G 5%
- Luhya (Kenya)A;A 99% A;G <1% G;G 0%
- Mexican ancestry (Los Angeles)A;A 41% A;G 45% G;G 14%
- Maasai (Kenya)A;A 96% A;G 4% G;G 0%
- TuscanA;A 35% A;G 54% G;G 11%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs10492519 is one of seven SNPs found in a combined study of over 1,000 patients to be associated with increased risk for prostate cancer. The risk allele for this SNP is (G); and while the odds ratio was not specifically reported, the probability of false significance (not permuted though) was given as p=5.6 x 10e-6, using an additive model of risk.
Source and license
Adapted from rs10492519 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.