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Vitiligo

UBASH3A · rs11203203

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Vitiligo compared to the general population. (GWAS Catalog, N Engl J Med 2010, PMID:20410501)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Vitiligo. (GWAS Catalog, N Engl J Med 2010, PMID:20410501)
G/G Published research associates this genotype with typical/baseline likelihood of Vitiligo — no copies of the reported risk allele. (GWAS Catalog, N Engl J Med 2010, PMID:20410501)

Source: GWAS Catalog, N Engl J Med 2010, PMID:20410501

Questions about rs11203203

What is rs11203203?

rs11203203 is a single position in the genome, in or near the UBASH3A gene. Published research associates it with vitiligo. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11203203 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 rs11203203 come from?

GWAS Catalog, N Engl J Med 2010, PMID:20410501. 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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