rs7927894
A SNP on chromosome 11. Its most notable genotype is C;C: 0.83x lower risk of Atopic Dermatitis.
- Gene
- None listed
- Location
- Chr 1176,590,272 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 28%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CMost notableGood0.83x lower risk of Atopic Dermatitis.
- C;TGoodNormal risk of Atopic Dermatitis.
- T;TBad1.2x higher risk of Atopic Dermatitis.
On SNPedia: (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.
- AverageC;C 52% C;T 39% T;T 8%
- European ancestry (Utah)C;C 39% C;T 43% T;T 18%
- Han Chinese (Beijing)C;C 63% C;T 33% T;T 4%
- Japanese (Tokyo)C;C 72% C;T 27% T;T 2%
- Yoruba (Nigeria)C;C 47% C;T 42% T;T 11%
- African ancestry (Southwest US)C;C 42% C;T 56% T;T 2%
- Chinese (Denver)C;C 62% C;T 35% T;T 4%
- Gujarati IndianC;C 57% C;T 35% T;T 8%
- Luhya (Kenya)C;C 53% C;T 38% T;T 9%
- Mexican ancestry (Los Angeles)C;C 55% C;T 38% T;T 7%
- Maasai (Kenya)C;C 52% C;T 38% T;T 10%
- TuscanC;C 34% C;T 49% T;T 17%
Notes
From SNPedia
Notes
23andMe blog associated rs7927894(T) with Crohn’s disease 1.16x and atopic dermatitis
C;C
Verified in Asians.
T;T
Verified in Asians.
Source and license
Adapted from rs7927894 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.