rs391300
A SNP in the SRR gene on chromosome 17. Its most notable genotype is T;T: 1.86x risk for gestational diabetes
- Gene
- SRR
- Location
- Chr 172,312,964 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 38%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TMost notableBad1.86x risk for gestational diabetes
- C;TNot rated1x risk for gestational diabetes
- C;CGoodnormal
SNPedia records rs391300 on the minus strand: (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.
- AverageT;T 19% C;T 47% C;C 34%
- European ancestry (Utah)T;T 13% C;T 47% C;C 40%
- Han Chinese (Beijing)T;T 6% C;T 38% C;C 57%
- Japanese (Tokyo)T;T 5% C;T 35% C;C 61%
- Yoruba (Nigeria)T;T 32% C;T 52% C;C 16%
- African ancestry (Southwest US)T;T 19% C;T 60% C;C 21%
- Chinese (Denver)T;T 18% C;T 46% C;C 36%
- Gujarati IndianT;T 25% C;T 54% C;C 22%
- Luhya (Kenya)T;T 30% C;T 49% C;C 21%
- Mexican ancestry (Los Angeles)T;T 9% C;T 45% C;C 47%
- Maasai (Kenya)T;T 32% C;T 48% C;C 20%
- TuscanT;T 22% C;T 49% C;C 30%
Source and license
Adapted from rs391300 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.