rs3821236
A SNP in the STAT4 gene on chromosome 2. Its most notable genotype is A;A: 2x higher risk of lupus
- Gene
- STAT4
- Location
- Chr 2191,038,032 (GRCh38)
- Highest magnitude
- 2.1Worth knowing
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 31%
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 12% A;G 43% G;G 46%
- European ancestry (Utah)A;A 5% A;G 33% G;G 62%
- Han Chinese (Beijing)A;A 20% A;G 52% G;G 29%
- Japanese (Tokyo)A;A 20% A;G 43% G;G 37%
- Yoruba (Nigeria)A;A 10% A;G 41% G;G 49%
- African ancestry (Southwest US)A;A 11% A;G 40% G;G 49%
- Chinese (Denver)A;A 17% A;G 54% G;G 28%
- Gujarati IndianA;A 4% A;G 35% G;G 61%
- Luhya (Kenya)A;A 8% A;G 48% G;G 44%
- Mexican ancestry (Los Angeles)A;A 26% A;G 52% G;G 22%
- Maasai (Kenya)A;A 5% A;G 39% G;G 57%
- TuscanA;A 2% A;G 33% G;G 65%
Related
Other STAT4 SNPs
- rs7574865T;T1.69x risk of rheumatoid arthritis; 2.4x risk of SLE; 2.28x risk of Sjögren's syndrome; increased risk of type-1 diabetes; and increased risk of primary biliary cirrhosis.Important
- rs10181656G;G1.7x increased SLE riskWorth knowing
- rs3024866G;Gcommon in clinvarTypical
- rs7582694C;C1.71x increased SLE riskTypical
- rs10168266C;Cnormal risk of Sjogren's syndromeTypical
Notes
From SNPedia
Notes
CPMC uses this to indicate increased risk of Systemic lupus erythematosus.
A;A
increased risk of Systemic lupus erythematosus.
A;G
increased risk of Systemic lupus erythematosus.
Source and license
Adapted from rs3821236 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.