rs17855765
A SNP in the SLC39A4 gene on chromosome 8. Its most notable genotype is C;C: common in clinvar
- Gene
- SLC39A4
- Location
- Chr 8144,415,944 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
- Minor allele frequency
- 43%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageC;C 40%
- European ancestry (Utah)C;C 31%
- Han Chinese (Beijing)C;C 29%
- Japanese (Tokyo)C;C 41%
- Yoruba (Nigeria)C;C 59%
Related
Other SLC39A4 SNPs
- rs121434287A;GCarrier of an acrodermatitis enteropathica mutationImportant
- rs121434288C;TCarrier of an acrodermatitis enteropathica mutationImportant
- rs121434289C;TCarrier of an acrodermatitis enteropathica mutationImportant
- rs121434290G;TCarrier of an acrodermatitis enteropathica mutationImportant
- rs121434291C;TCarrier of an acrodermatitis enteropathica mutationImportant
- rs121434292A;GCarrier of an acrodermatitis enteropathica mutationImportant
- rs121434293C;GCarrier of an acrodermatitis enteropathica mutationImportant
- rs782695425-;GCarrier of a likely acrodermatitis enteropathica mutationImportant
Source and license
Adapted from rs17855765 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.