Sensitive

Basal cell carcinoma (PheCode 172.21)

near BNC2 · rs369593216

Where this position leads

Condition: Basal Cell Carcinoma

rs369593216 Condition: Basal Cell Carcinoma Basal Cell Carcinoma Condition rs369593216 rs369593216 near BNC2

What the study found

Who was studied 768 Hispanic or Latin American cases, 58,733 Hispanic or Latin American controls, 31,142 European ancestry cases, 404,406 European ancestry controls.

The effect Each copy of the T allele shifted the measure 0.117 lower (95% confidence interval 0.1-0.135); p = 2 × 10−30.

How common The T allele had a frequency of about 48% in the people studied.

Where it sits Chromosome 9, band 9p22.2 — between genes, 5.9 kb from BNC2.

What each result means

C/C No copy of the version the research linked to Basal cell carcinoma (PheCode 172.21). This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Basal cell carcinoma (PheCode 172.21). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Basal cell carcinoma (PheCode 172.21). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs369593216

What is rs369593216?

rs369593216 is a single position in the genome, in or near the near BNC2 gene. Published research associates it with basal cell carcinoma (phecode 172.21). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs369593216 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 rs369593216 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 rs369593216 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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.

Basal cell carcinoma (PheCode 172.21) (rs369593216). MyGeneLog™. https://www.mygenelog.com/variants/rs369593216

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