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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 14,694 European ancestry cases, 150,563 European ancestry controls.
The effect
Each copy of the G allele carried 0.79 times the odds of Cervical dysplasia (95% confidence interval 0.76-0.83); p = 2 × 10−22.
How common The G allele had a frequency of about 9% in the people studied.
Where it sits Chromosome 6, band 6p21.32 — inside HLA-DQA1.
What each result means
G/GTwo copies of the version the research linked to Cervical dysplasia. That is the strongest link of the three results. A link in a study is not a diagnosis.
G/TOne copy of the version the research linked to Cervical dysplasia. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Cervical dysplasia. This is the starting point the study compared everyone against.
Human molecular genetics · 2023 · PMID 36929174 · open access
Questions about rs36214159
What is rs36214159?
rs36214159 is a single position in the genome, in or near the HLA-DQA1 gene. Published research associates it with cervical dysplasia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs36214159 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 rs36214159 come from?
GWAS Catalog, Human molecular genetics 2023, PMID:36929174. 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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