rs4027132
A SNP on chromosome 2. Its most notable genotype is A;A: 1.51x increased risk of developing bipolar disorder
- Gene
- None listed
- Location
- Chr 211,897,366 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 47%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBad1.51x increased risk of developing bipolar disorder
- A;GBad1.39x increased risk of developing bipolar disorder
- G;GGoodNormal risk of developing bipolar disorder
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 28% A;G 50% G;G 22%
- European ancestry (Utah)A;A 31% A;G 53% G;G 16%
- Han Chinese (Beijing)A;A 26% A;G 50% G;G 25%
- Japanese (Tokyo)A;A 24% A;G 48% G;G 28%
- Yoruba (Nigeria)A;A 31% A;G 46% G;G 23%
- African ancestry (Southwest US)A;A 23% A;G 56% G;G 21%
- Chinese (Denver)A;A 16% A;G 51% G;G 34%
- Gujarati IndianA;A 32% A;G 47% G;G 22%
- Luhya (Kenya)A;A 28% A;G 55% G;G 17%
- Mexican ancestry (Los Angeles)A;A 33% A;G 40% G;G 28%
- Maasai (Kenya)A;A 34% A;G 50% G;G 16%
- TuscanA;A 30% A;G 53% G;G 17%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs4027132 has been reported in a large study to be associated with bipolar disorder. The risk allele (oriented to the dbSNP entry) is (A), and the odds ratio associated with heterozygotes is 1.39 (CI 1.19-1.64), and for homozygotes, 1.51 (CI 1.27-1.79).
Source and license
Adapted from rs4027132 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.