rs4713902
A SNP in the FKBP5 gene on chromosome 6. Its most notable genotype is C;C: 0.47x decreased risk for bipolar disorder
- Gene
- FKBP5
- Location
- Chr 635,646,249 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 24%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CMost notableGood0.47x decreased risk for bipolar disorder
- C;TGood0.69x decreased risk for bipolar disorder
- T;TNot ratednormal
On SNPedia: (C;C), (C;T), (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.
- AverageC;C 6% C;T 32% T;T 62%
- European ancestry (Utah)C;C 6% C;T 37% T;T 57%
- Han Chinese (Beijing)C;C 7% C;T 37% T;T 56%
- Japanese (Tokyo)C;C 10% C;T 37% T;T 53%
- Yoruba (Nigeria)C;C 0% C;T 13% T;T 87%
- African ancestry (Southwest US)C;C 2% C;T 28% T;T 70%
- Chinese (Denver)C;C 5% C;T 35% T;T 61%
- Gujarati IndianC;C 2% C;T 31% T;T 67%
- Luhya (Kenya)C;C 0% C;T 12% T;T 88%
- Mexican ancestry (Los Angeles)C;C 19% C;T 59% T;T 22%
- Maasai (Kenya)C;C 5% C;T 32% T;T 64%
- TuscanC;C 12% C;T 36% T;T 52%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs4713902, a SNP in the FKBP5 gene, is associated with increased risk for bipolar disorder in a study of 500+ Caucasian patients. The most common allele, rs4713902(T), was associated with highest risk. Giving that allele a relative odds ratio of 1.0, the odds for the (C;T) and (C;C) genotypes were 0.69x (CI:0.55-0.88, p=0.001) and 0.47 (CI: 0.30-0.74, p=0.001).
Source and license
Adapted from rs4713902 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.