rs5744241
A SNP in the IL18 gene on chromosome 11. Its most notable genotype is T;T: common in complete genomics
- Gene
- IL18
- Location
- Chr 11112,156,421 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
- Minor allele frequency
- 4%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs5744241 on the minus strand: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 6 HapMap populations.
- AverageT;T 93%
- European ancestry (Utah)T;T 80%
- African ancestry (Southwest US)T;T 98%
- Gujarati IndianT;T 96%
- Mexican ancestry (Los Angeles)T;T 93%
- Maasai (Kenya)T;T 99%
- TuscanT;T 91%
Related
Source and license
Adapted from rs5744241 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.