1 2521612328Reads by AI crawlersClaude0ChatGPT2Google · Gemini0Perplexity1Meta AI6Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others8Total25Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Who was studied 31,787 European ancestry cases, 619,351 European ancestry controls.
The effect
Each copy of the C allele carried 1.05 times the odds of Basal cell carcinoma (95% confidence interval 1.04-1.08); p = 2 × 10−9.
How common The C allele had a frequency of about 69% in the people studied.
Where it sits Chromosome 8, band 8q22.1 — in a regulatory region of LOC101927066.
What each result means
C/CTwo copies of the version the research linked to Basal cell carcinoma. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Basal cell carcinoma. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Basal cell carcinoma. This is the starting point the study compared everyone against.
Human molecular genetics · 2019 · PMID 31174203 · open access
Questions about rs7833199
What is rs7833199?
rs7833199 is a single position in the genome, in or near the U3 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.
What conditions is rs7833199 linked to?
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.
Does having rs7833199 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 rs7833199 come from?
GWAS Catalog, Hum Mol Genet 2019, PMID:31174203. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
1 2521612328Reads by AI crawlersClaude0ChatGPT2Google · Gemini0Perplexity1Meta AI6Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others8Total25Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Quoting this page
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.