rs2834167
A SNP in the IL10RB gene on chromosome 21. Its most notable genotype is A;A: 2.67x increased risk for systemic sclerosis
- Gene
- IL10RB
- Location
- Chr 2133,268,483 (GRCh38)
- Highest magnitude
- 2.1Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 34%
Genotypes
As shown in 23andMe and AncestryDNA files.
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 51% A;G 35% G;G 15%
- European ancestry (Utah)A;A 53% A;G 42% G;G 5%
- Han Chinese (Beijing)A;A 20% A;G 44% G;G 36%
- Japanese (Tokyo)A;A 25% A;G 53% G;G 22%
- Yoruba (Nigeria)A;A 82% A;G 17% G;G <1%
- African ancestry (Southwest US)A;A 77% A;G 21% G;G 2%
- Chinese (Denver)A;A 25% A;G 39% G;G 36%
- Gujarati IndianA;A 33% A;G 50% G;G 18%
- Luhya (Kenya)A;A 86% A;G 12% G;G 2%
- Mexican ancestry (Los Angeles)A;A 21% A;G 48% G;G 31%
- Maasai (Kenya)A;A 77% A;G 23% G;G 0%
- TuscanA;A 59% A;G 32% G;G 9%
Related
Conditions, medicines and genes
Notes
From SNPedia
Show notes, about 150 words
rs2834167 is a SNP in the interleukin-10 receptor 2 IL10RB gene. In a study of Japanese patients, rs2834167(A;A) individuals were at increased risk for diffuse cutaneous systemic sclerosis (odds ratio 2.67, p = 0.0018).
A;A
IL-10RB rs2834167 (A/G) polymorphism is associated with the susceptibility to systemic lupus erythematosus: evidence from a study in Chinese Han population. We found that the frequency of A allele for rs2834167 in patients (44.53 %) was significantly higher than in controls (40.16 %) (χ (2) = 5.24, P = 0.022). Allele A was associated with a 1.196-fold (95 % confidence interval (CI), 1.026-1.394) greater risk for the occurrence of SLE compared with the G allele. And both genotypes AG and AA were associated with the susceptibility to SLE as compared with the GG genotype (AG versus GG, odds ratio (OR) = 1.332; 95 %CI, 1.047-1.696; AA versus GG, OR = 1.373; 95 %CI, 1.004-1.878).
References
Source and license
Adapted from rs2834167 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.