rs1545985
A SNP in the FYCO1 gene on chromosome 3. Its most notable genotype is A;A: normal risk
- Gene
- FYCO1
- Location
- Chr 345,963,986 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 19%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableNot ratednormal risk
- A;GBadsomewhat higher risk for prostate cancer
- G;GBadsomewhat higher risk for prostate cancer
- T;TNot ratedNo summary available.
On SNPedia: (A;A), (A;G), (G;G), (T;T). 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 69% A;G 25% G;G 6% T;T 0%
- European ancestry (Utah)A;A 43% A;G 39% G;G 18% T;T 0%
- Han Chinese (Beijing)A;A 99% A;G <1% G;G 0% T;T 0%
- Japanese (Tokyo)A;A 100% A;G 0% G;G 0% T;T 0%
- Yoruba (Nigeria)A;A 74% A;G 24% G;G 2% T;T 0%
- African ancestry (Southwest US)A;A 61% A;G 35% G;G 4% T;T 0%
- Chinese (Denver)A;A 99% A;G <1% G;G 0% T;T 0%
- Gujarati IndianA;A 30% A;G 50% G;G 21% T;T 0%
- Luhya (Kenya)A;A 63% A;G 33% G;G 5% T;T 0%
- Mexican ancestry (Los Angeles)A;A 79% A;G 19% G;G 2% T;T 0%
- Maasai (Kenya)A;A 55% A;G 36% G;G 9% T;T 0%
- TuscanA;A 54% A;G 38% G;G 8% T;T 0%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs1545985 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=6.6 x 10e-6, using an additive model of risk.
Source and license
Adapted from rs1545985 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.