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Skin colour saturation

ASIP · rs6059655

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Skin colour saturation compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Skin colour saturation.
G/G Published research associates this genotype with typical/baseline likelihood of Skin colour saturation — no copies of the reported risk allele.
Source

Questions about rs6059655

What is rs6059655?

rs6059655 is a single position in the genome, in or near the ASIP gene. Published research associates it with skin colour saturation. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs6059655 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs6059655 come from?

GWAS Catalog, Hum Genet 2015, PMID:25963972. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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