rs2943641
A SNP on chromosome 2. Its most notable genotype is C;C: increased risk for type 2 diabetes
- Gene
- None listed
- Location
- Chr 2226,229,029 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 27%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C), (C;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 57% C;T 36%
- European ancestry (Utah)C;C 42% C;T 43%
- Han Chinese (Beijing)C;C 89% C;T 11%
- Japanese (Tokyo)C;C 87% C;T 13%
- Yoruba (Nigeria)C;C 57% C;T 39%
- African ancestry (Southwest US)C;C 47% C;T 47%
- Chinese (Denver)C;C 89% C;T 11%
- Gujarati IndianC;C 54% C;T 41%
- Luhya (Kenya)C;C 32% C;T 52%
- Mexican ancestry (Los Angeles)C;C 64% C;T 35%
- Maasai (Kenya)C;C 34% C;T 51%
- TuscanC;C 36% C;T 51%
Notes
From SNPedia
Notes
identified a significant association of rs2943641 near IRS1 locus, with type 2 diabetes in the Japanese population. Prioritizing genes for follow-up from genome wide association studies using information on gene expression in tissues relevant for type 2 diabetes mellitus. The type 2 diabetes and insulin-resistance locus near IRS1 is a determinant of HDL cholesterol and triglycerides levels among diabetic subjects. Insulin receptor substrate 1 gene variation modifies insulin resistance response to weight-loss diets in a 2-year randomized trial: the Preventing Overweight Using Novel Dietary Strategies (POUNDS LOST) trial.
Source and license
Adapted from rs2943641 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.