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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 21,385 European ancestry cases, 213,236 European ancestry controls.
The effect
Each copy of the T allele carried 1.08 times the odds of ICD10 N81: Female genital prolapse (95% confidence interval 1.05-1.1); p = 9 × 10−11.
Where it sits Chromosome 1, band 1p32.2 — between genes, 51.7 kb from RPSAP20.
What each result means
C/CNo copy of the version the research linked to ICD10 N81: Female genital prolapse. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to ICD10 N81: Female genital prolapse. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to ICD10 N81: Female genital prolapse. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs1935050 is a single position in the genome, in or near the near RPSAP20 gene. Published research associates it with icd10 n81: female genital prolapse. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1935050 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 rs1935050 come from?
GWAS Catalog, Nature medicine 2025, PMID:40069456. 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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