rs2278206
A SNP in the INPP4A gene on chromosome 2. Its most notable genotype is A;A: 1.16x increased risk for asthma
- Gene
- INPP4A
- Location
- Chr 298,555,781 (GRCh38)
- Highest magnitude
- 1.8Minor
- Tested on
- 23andMe
- Minor allele frequency
- 28%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- C;TNot ratedNo summary available.
- G;GGoodpossibly less susceptible to asthma
- A;GNot ratednormal
- A;AMost notableBad1.16x increased risk for asthma
SNPedia records rs2278206 on the minus strand: (A;G), (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;T 0% G;G 8% A;G 39% A;A 53%
- European ancestry (Utah)C;T 0% G;G 5% A;G 35% A;A 59%
- Han Chinese (Beijing)C;T 0% G;G 9% A;G 37% A;A 54%
- Japanese (Tokyo)C;T 0% G;G 8% A;G 43% A;A 49%
- Yoruba (Nigeria)C;T 0% G;G 3% A;G 26% A;A 71%
- African ancestry (Southwest US)C;T 0% G;G 9% A;G 37% A;A 54%
- Chinese (Denver)C;T 0% G;G 9% A;G 38% A;A 53%
- Gujarati IndianC;T 0% G;G 9% A;G 46% A;A 46%
- Luhya (Kenya)C;T 0% G;G 13% A;G 43% A;A 45%
- Mexican ancestry (Los Angeles)C;T 0% G;G 2% A;G 50% A;A 48%
- Maasai (Kenya)C;T 0% G;G 10% A;G 40% A;A 51%
- TuscanC;T 0% G;G 11% A;G 40% A;A 49%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
A study of ~170 families led to a slight association between rs2278206 and atopic asthma. The risk genotype - in dbSNP orientation, not as published - is rs2278206(T;T). Conversely, the rs2278206(C;C) genotype was rarely (odds ratio 0.13) seen in patients with atopic asthma.
Source and license
Adapted from rs2278206 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.