rs2227532
A SNP in the IL8 gene on chromosome 4. Its most notable genotype is T;T: common in complete genomics
- Gene
- IL8
- Location
- Chr 473,739,815 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 2%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 7 HapMap populations.
- AverageT;T 90%
- Yoruba (Nigeria)T;T 78%
- African ancestry (Southwest US)T;T 84%
- Gujarati IndianT;T 96%
- Luhya (Kenya)T;T 96%
- Mexican ancestry (Los Angeles)T;T 95%
- Maasai (Kenya)T;T 80%
- TuscanT;T 99%
Notes
From SNPedia
Notes
The chemokine network. II. On how polymorphisms and alternative splicing increase the number of molecular species and configure intricate patterns of disease susceptibility.
Source and license
Adapted from rs2227532 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.