DHX36 · rs9823832
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 31,374 European ancestry cases, 414,052 European ancestry controls.
The effect Each copy of the C allele shifted the measure 0.114 lower (95% confidence interval 0.097-0.132); p = 9 × 10−37.
How common The C allele had a frequency of about 34% in the people studied.
Where it sits Chromosome 3, band 3q25.2 — in an intron of DHX36.
rs9823832 is a single position in the genome, in or near the DHX36 gene. Published research associates it with epiretinal membrane. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
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, Cell genomics 2024, PMID:38870908. 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.
Epiretinal membrane (rs9823832). MyGeneLog™. https://www.mygenelog.com/variants/rs9823832