RHOU · rs801108
Where this position leads
Condition: Basal Cell Carcinoma
What the study found
Who was studied 17,416 European ancestry cases, 375,455 European ancestry controls.
The effect Each copy of the G allele shifted the measure 0.215 higher (95% confidence interval 0.19-0.24); p = 1 × 10−71.
How common The G allele had a frequency of about 25% in the people studied.
Where it sits Chromosome 1, band 1q42.13 — between genes, 76.5 kb from LOC100421842.
rs801108 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.
On MyGeneLog this position is linked to Basal Cell Carcinoma. The research behind each link, and its sources, are set out on that condition page.
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.
GWAS Catalog, Genome Med 2021, PMID:33549134. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Basal cell carcinoma (rs801108). MyGeneLog™. https://www.mygenelog.com/variants/rs801108