rs140504
A SNP in the BCR gene on chromosome 22. Its most notable genotype is A;A: 1.4x increased risk for bipolar disorder
- Gene
- BCR
- Location
- Chr 2223,285,182 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 20%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableNot rated1.4x increased risk for bipolar disorder
- A;GBad1.4x increased risk for bipolar disorder
- G;GNot ratednormal risk
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 7% A;G 25% G;G 68%
- European ancestry (Utah)A;A <1% A;G 25% G;G 74%
- Han Chinese (Beijing)A;A 23% A;G 50% G;G 27%
- Japanese (Tokyo)A;A 23% A;G 49% G;G 28%
- Yoruba (Nigeria)A;A 0% A;G 4% G;G 96%
- African ancestry (Southwest US)A;A 0% A;G 23% G;G 77%
- Chinese (Denver)A;A 23% A;G 48% G;G 29%
- Gujarati IndianA;A 4% A;G 37% G;G 59%
- Luhya (Kenya)A;A 0% A;G 7% G;G 93%
- Mexican ancestry (Los Angeles)A;A 2% A;G 14% G;G 84%
- Maasai (Kenya)A;A 1% A;G 7% G;G 92%
- TuscanA;A 2% A;G 15% G;G 83%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs140504, a SNP in the BCR gene on chromosome 22, has been associated with increased risk for bipolar disorder. The odds ratio for carriers of the minor allele (G) are reported as 1.45 (CI:1.11 - 1.84, p=0.0054) based on a study of 171 Japanese patients.
Source and license
Adapted from rs140504 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.