rs2609653
A SNP on chromosome 8. Its most notable genotype is A;A.
- Gene
- None listed
- Location
- Chr 834,379,474 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 5%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableNot ratedNo summary available.
- C;CNot rated3.6x risk
- C;TNot rated1.5x risk
- T;TGoodnormal
On SNPedia: (A;A), (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.
- AverageA;A 0% C;C <1% C;T 8% T;T 91%
- European ancestry (Utah)A;A 0% C;C <1% C;T 9% T;T 90%
- Han Chinese (Beijing)A;A 0% C;C 0% C;T 10% T;T 90%
- Japanese (Tokyo)A;A 0% C;C 0% C;T 7% T;T 93%
- Yoruba (Nigeria)A;A 0% C;C <1% C;T 13% T;T 86%
- African ancestry (Southwest US)A;A 0% C;C 2% C;T 7% T;T 91%
- Chinese (Denver)A;A 0% C;C 0% C;T 16% T;T 84%
- Gujarati IndianA;A 0% C;C 0% C;T 2% T;T 98%
- Luhya (Kenya)A;A 0% C;C 0% C;T 8% T;T 92%
- Mexican ancestry (Los Angeles)A;A 0% C;C 0% C;T 3% T;T 97%
- Maasai (Kenya)A;A 0% C;C 0% C;T 8% T;T 92%
- TuscanA;A 0% C;C 0% C;T 8% T;T 92%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs2609653 has been reported in a large study to be associated with bipolar disorder. The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 1.43 (CI 1.19-1.71), and for homozygotes, 3.62 (CI 1.26-10.44).
Source and license
Adapted from rs2609653 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.