rs2303067
A SNP in the SPINK5 gene on chromosome 5. Its most notable genotype is A;A: 1.8x risk
- Gene
- SPINK5
- Location
- Chr 5148,101,392 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 43%
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 37% A;G 44% G;G 18%
- European ancestry (Utah)A;A 26% A;G 52% G;G 22%
- Han Chinese (Beijing)A;A 29% A;G 46% G;G 25%
- Japanese (Tokyo)A;A 27% A;G 57% G;G 16%
- Yoruba (Nigeria)A;A 65% A;G 32% G;G 3%
- African ancestry (Southwest US)A;A 51% A;G 42% G;G 7%
- Chinese (Denver)A;A 21% A;G 54% G;G 25%
- Gujarati IndianA;A 26% A;G 53% G;G 22%
- Luhya (Kenya)A;A 65% A;G 28% G;G 7%
- Mexican ancestry (Los Angeles)A;A 14% A;G 35% G;G 52%
- Maasai (Kenya)A;A 56% A;G 38% G;G 6%
- TuscanA;A 29% A;G 54% G;G 17%
Related
Conditions, medicines and genes
Notes
From SNPedia
Show notes, about 120 words
rs2303067, a SNP in the SPINK5 gene, has been significantly associated with susceptibility to atopic dermatitis. The risk allele for rs2303067 is (A). rs2303067 has also been associated with predisposition to asthma, . From this study: "A significant association between rs2303067 and the development of asthma was observed (OR 1.77; 95%CI: 1.02-3.06, P=0.041 for rs2303067(A;A) homozygotes). Atopic carriers of rs2303067 showed an increased risk for asthma and asthma symptoms (OR 2.06; 95%CI: 1.01-4.20, P=0.047). When children with a combination of asthma and atopic dermatitis were compared with normal controls, the rs2303067(A) genotype was more prevalent in the disease group (OR 4.56; 95%CI: 1.370-15.12, P=0.007)."
Source and license
Adapted from rs2303067 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.