rs11755699
A SNP in the SGK1 gene on chromosome 6. Its most notable genotype is T;T: common genotype
- Gene
- SGK1
- Location
- Chr 6134,278,109 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 4%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 9 HapMap populations.
- AverageT;T 94%
- European ancestry (Utah)T;T 82%
- Han Chinese (Beijing)T;T 100%
- Japanese (Tokyo)T;T 100%
- Yoruba (Nigeria)T;T 100%
- African ancestry (Southwest US)T;T 98%
- Gujarati IndianT;T 95%
- Mexican ancestry (Los Angeles)T;T 90%
- Maasai (Kenya)T;T 97%
- TuscanT;T 87%
Related
Conditions, medicines and genes
Other SGK1 SNPs
Genosets
Genosets combine several genotypes. Twofold checks them in your report.
Notes
From SNPedia
Notes
see gs248 patented by 23andMe to diagnose Parkinson's disease
Source and license
Adapted from rs11755699 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.