rs7570682
A SNP on chromosome 2. Its most notable genotype is A;A: 1.6x risk
- Gene
- None listed
- Location
- Chr 2104,366,809 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 33%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A), (A;G), (C;C), (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 15% A;G 42% C;C 0% G;G 43%
- European ancestry (Utah)A;A 4% A;G 40% C;C 0% G;G 57%
- Han Chinese (Beijing)A;A 10% A;G 50% C;C 0% G;G 40%
- Japanese (Tokyo)A;A 11% A;G 44% C;C 0% G;G 46%
- Yoruba (Nigeria)A;A 20% A;G 54% C;C 0% G;G 26%
- African ancestry (Southwest US)A;A 40% A;G 39% C;C 0% G;G 21%
- Chinese (Denver)A;A 16% A;G 43% C;C 0% G;G 41%
- Gujarati IndianA;A 0% A;G 21% C;C 0% G;G 79%
- Luhya (Kenya)A;A 28% A;G 51% C;C 0% G;G 21%
- Mexican ancestry (Los Angeles)A;A 5% A;G 43% C;C 0% G;G 52%
- Maasai (Kenya)A;A 26% A;G 44% C;C 0% G;G 30%
- TuscanA;A 4% A;G 31% C;C 0% G;G 65%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs7570682 has been reported in a large study to be associated with bipolar disorder. The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with heterozygotes is 1.23 (CI 1.09-1.40), and for homozygotes, 1.64 (CI 1.28-2.12).
Source and license
Adapted from rs7570682 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.