rs2295490
A SNP in the TRIB3 gene on chromosome 20. Its most notable genotype is A;G: 1.32x increased risk of early-onset type-2 diabetes
- Gene
- TRIB3
- Location
- Chr 20388,261 (GRCh38)
- Highest magnitude
- 1.3Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 16%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AGoodnormal
- A;GMost notableBad1.32x increased risk of early-onset type-2 diabetes
- G;GBad1.32x increased risk of early-onset type-2 diabetes
On SNPedia: (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.
- AverageA;A 67% A;G 30% G;G 3%
- European ancestry (Utah)A;A 77% A;G 21% G;G 3%
- Han Chinese (Beijing)A;A 60% A;G 36% G;G 5%
- Japanese (Tokyo)A;A 56% A;G 39% G;G 5%
- Yoruba (Nigeria)A;A 73% A;G 24% G;G 3%
- African ancestry (Southwest US)A;A 72% A;G 28% G;G 0%
- Chinese (Denver)A;A 71% A;G 27% G;G 3%
- Gujarati IndianA;A 39% A;G 49% G;G 12%
- Luhya (Kenya)A;A 68% A;G 29% G;G 3%
- Mexican ancestry (Los Angeles)A;A 91% A;G 9% G;G 0%
- Maasai (Kenya)A;A 58% A;G 38% G;G 5%
- TuscanA;A 70% A;G 29% G;G 1%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs2295490 is a SNP in the tribbles homolog 3 TRIB3 gene, also known as Q84R. The (A) allele encodes the Gln (Q), while the (G) allele encodes the Arg (R). A study involving four different case-control samples comprising a total of 5469 Caucasisans determined that rs2295490(G) was nominally associated with type-2 diabetes (odds ratio 1.17, CI: 1.00-1.36, p = 0.04). When stratified by age of diabetes onset, these carriers had an increased risk of early-onset T2D (OR 1.32, CI: 1.10-1.58, p = 0.002). this gain of function mutation may affect insulin signaling and increase the risk of insulin resistance
A;A
Normal risk of early-onset type II diabetes
Source and license
Adapted from rs2295490 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.