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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 the study found
Who was studied 367 European ancestry cases, 31,563 European ancestry controls.
The effect
Each copy of the G allele carried 8.49 times the odds of Familial squamous cell lung carcinoma (95% confidence interval 4.12-17.49); p = 6 × 10−9.
How common The G allele had a frequency of about 0% in the people studied.
Where it sits Chromosome 9, band 9p21.3 — between genes, 25.1 kb from KHSRPP1.
What each result means
A/ANo copy of the version the research linked to Familial squamous cell lung carcinoma. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Familial squamous cell lung carcinoma. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Familial squamous cell lung carcinoma. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs12686364 is a single position in the genome, in or near the near KHSRPP1 gene. Published research associates it with familial squamous cell lung carcinoma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs12686364 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 rs12686364 come from?
GWAS Catalog, Carcinogenesis 2018, PMID:29924316. 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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