Sensitive

Basal cell carcinoma

RHOU · rs801114

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What each result means

G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Basal cell carcinoma compared to the general population. (GWAS Catalog, Nat Commun 2015, PMID:25855136)

G/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Basal cell carcinoma. (GWAS Catalog, Nat Commun 2015, PMID:25855136)

T/T Published research associates this genotype with typical/baseline likelihood of Basal cell carcinoma — no copies of the reported risk allele. (GWAS Catalog, Nat Commun 2015, PMID:25855136)

Source: GWAS Catalog, Nat Commun 2015, PMID:25855136

Questions about rs801114

What is rs801114?

rs801114 is a single position in the genome, in or near the RHOU gene. Published research associates it with basal cell carcinoma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs801114 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 rs801114 come from?

GWAS Catalog, Nat Commun 2015, PMID:25855136. 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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