rs2074190
A SNP in the TBX21 gene on chromosome 17. Its most notable genotype is G;G: 2.2x risk for AIA
- Gene
- TBX21
- Location
- Chr 1747,733,844 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 24%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2074190 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 8% A;G 36% A;A 56%
- European ancestry (Utah)G;G 4% A;G 39% A;A 57%
- Han Chinese (Beijing)G;G 2% A;G 19% A;A 79%
- Japanese (Tokyo)G;G <1% A;G 12% A;A 87%
- Yoruba (Nigeria)G;G 10% A;G 43% A;A 47%
- African ancestry (Southwest US)G;G 11% A;G 34% A;A 55%
- Chinese (Denver)G;G <1% A;G 18% A;A 81%
- Gujarati IndianG;G 12% A;G 45% A;A 44%
- Luhya (Kenya)G;G 7% A;G 43% A;A 50%
- Mexican ancestry (Los Angeles)G;G 9% A;G 56% A;A 35%
- Maasai (Kenya)G;G 18% A;G 49% A;A 33%
- TuscanG;G 15% A;G 33% A;A 52%
Related
Conditions, medicines and genes
Other TBX21 SNPs
- rs4794067C;C2.1x risk for Aspirin Induced Asthma. But possibly lower risk of lupus and intractable Graves' disease.Worth knowing
- rs11650354T;T8x risk for allergic asthmaWorth knowing
- rs17250932C;CReduced risk of lupus and intractable Graves' disease.Worth knowing
- rs2240017G;Gnot observed (too rare)Typical
- rs16947078A;AcommonTypical
Notes
From SNPedia
Notes
rs2074190(G;G) and rs2074190(A;G) genotypes for the TBX21 gene are calculated to be at 2.19 fold higher risk (CI: 1.27-3.77) for aspirin-induced asthma (AIA) compared to rs2074190(A;A) homozygotes, based on a study of 72 patients vs 640 controls in a study of a Japanese population. Note that in this population, but perhaps not others, linkage disequilibrium exists between this SNP located in the first exon, rs2074190, and a SNP located upstream of the gene, rs4794067, with a predictive accuracy of 92%.
Source and license
Adapted from rs2074190 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.