rs7216389
A SNP in the GSDMB gene on chromosome 17. Its most notable genotype is C;C: 0.69x lower risk of Childhood Asthma.
- Gene
- GSDMB
- Location
- Chr 1739,913,696 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 37%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CMost notableGood0.69x lower risk of Childhood Asthma.
- C;TNot ratedNormal risk for Childhood Asthma.
- T;TBad1.5x increased risk for Childhood Asthma.
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 11% C;T 40% T;T 49%
- European ancestry (Utah)C;C 24% C;T 55% T;T 21%
- Han Chinese (Beijing)C;C 10% C;T 47% T;T 43%
- Japanese (Tokyo)C;C 8% C;T 41% T;T 51%
- Yoruba (Nigeria)C;C 2% C;T 20% T;T 78%
- African ancestry (Southwest US)C;C 9% C;T 42% T;T 49%
- Chinese (Denver)C;C 7% C;T 39% T;T 54%
- Gujarati IndianC;C 17% C;T 46% T;T 38%
- Luhya (Kenya)C;C 2% C;T 21% T;T 77%
- Mexican ancestry (Los Angeles)C;C 17% C;T 45% T;T 38%
- Maasai (Kenya)C;C 3% C;T 30% T;T 68%
- TuscanC;C 21% C;T 55% T;T 25%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs7216389, a SNP in the ORMDL3 gene on chromosome 17q21, was associated with susceptibility to childhood asthma in a study of ~1,000 British patients. The variation appears to be linked to altered levels of the ORMDL3 mRNA, which was shown in a cohort study of ~5,000 British and German patients to be correlated to childhood asthma. A large study of Scottish asthma patients replicated these results, finding that a single copy of the T allele conferred an odds ratio of 1.50 (CI: 1.24-1.81) and 2 copies conferred an odds ratio of 2.11 (CI: 1.71-2.61), respectively.
Source and license
Adapted from rs7216389 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.