rs9402571
A SNP in the SGK1 gene on chromosome 6. Its most notable genotype is G;G: 0.85x decreased risk for type-2 diabetes
- Gene
- SGK1
- Location
- Chr 6134,167,822 (GRCh38)
- Highest magnitude
- 1.8Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 26%
Genotypes
As shown in 23andMe and AncestryDNA files.
- G;GMost notableGood0.85x decreased risk for type-2 diabetes
- G;TGoodslightly decreased risk for type-2 diabetes
- T;TNot ratednormal
On SNPedia: (G;G), (G;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.
- AverageG;G 8% G;T 36% T;T 56%
- European ancestry (Utah)G;G 4% G;T 26% T;T 70%
- Han Chinese (Beijing)G;G 15% G;T 50% T;T 35%
- Japanese (Tokyo)G;G 14% G;T 41% T;T 44%
- Yoruba (Nigeria)G;G 8% G;T 35% T;T 57%
- African ancestry (Southwest US)G;G 11% G;T 35% T;T 54%
- Chinese (Denver)G;G 15% G;T 51% T;T 34%
- Gujarati IndianG;G 2% G;T 30% T;T 68%
- Luhya (Kenya)G;G 7% G;T 40% T;T 53%
- Mexican ancestry (Los Angeles)G;G 3% G;T 24% T;T 72%
- Maasai (Kenya)G;G 8% G;T 30% T;T 62%
- TuscanG;G 5% G;T 31% T;T 64%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs9402571 is a SNP in the serum/glucocorticoid regulated kinase 1 SGK1 gene. Three independent European populations were analyzed, with follow up in 3798 non-diabetic and 659 diabetic (type 2) individuals, for associations between SGK1 SNPs and insulin secretion. In lean non-diabetic individuals, rs9402571(G) minor allele carriers had higher (better) insulin response and lower prevalence of type-2 diabetes, with an odds ratio of 0.85 (CI: 0.7-1.0, p = .065, dominant model).
Source and license
Adapted from rs9402571 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.