rs5275
NM_000963.4(PTGS2):c.*427T>C
- Cholangiocarcinomaother · germline
gnomAD allele frequency 4.01e-1
rs5275 is a genetic variant located in the PTGS2 gene. dbsnp · gene
In gnomAD, rs5275 has an overall allele frequency of 40.1%. gnomad · frequency
In ClinVar, rs5275 is classified as other for Cholangiocarcinoma (0 review stars, germline; last evaluated 2022-12-10). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
retrieved 2026-08-03 · facts 0cb088e41dd3e604 · meta/llama-3.1-8b-instruct · prompt 4.0.1 · schema 3.0.0
Educational information only — not medical advice, a diagnosis, or a clinical interpretation. A variant's significance can be uncertain, conflicting, or dependent on your full clinical and family context. Consult a qualified genetics professional or genetic counselor before drawing any conclusion.