rs1889018
A SNP in the SREBF1 gene on chromosome 17. Its most notable genotype is G;G: normal
- Gene
- SREBF1
- Location
- Chr 1717,831,426 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 32%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GMost notableNot ratednormal
- A;GNot rated1.12x increased risk for T2D
- A;ANot rated1.12x increased risk for T2D
SNPedia records rs1889018 on the minus strand: (C;C), (C;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 61% A;G 29% A;A 10%
- European ancestry (Utah)G;G 11% A;G 41% A;A 49%
- Han Chinese (Beijing)G;G 91% A;G 9% A;A <1%
- Japanese (Tokyo)G;G 88% A;G 12% A;A <1%
- Yoruba (Nigeria)G;G 82% A;G 17% A;A <1%
- African ancestry (Southwest US)G;G 61% A;G 32% A;A 7%
- Chinese (Denver)G;G 94% A;G 6% A;A <1%
- Gujarati IndianG;G 58% A;G 37% A;A 5%
- Luhya (Kenya)G;G 77% A;G 22% A;A <1%
- Mexican ancestry (Los Angeles)G;G 28% A;G 52% A;A 21%
- Maasai (Kenya)G;G 65% A;G 35% A;A 0%
- TuscanG;G 19% A;G 56% A;A 26%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs1889018 is one of several SNPs associated with the SREBF1 gene that show a modest association with type-2 diabetes. A study of ~2,000 Caucasian patients (and 10,000+ controls) led to an odds ratio of 1.12 (CI: 1.01-1.24, p=0.04) for the minor (risk) allele, rs1889018(T). This allele was also associated with a surrogate measure of insulin sensitivity (p=0.03).
Source and license
Adapted from rs1889018 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.