rs1333049
NC_000009.12:g.22125504G>C
- Three Vessel Coronary DiseaseRisk factor · somatic
gnomAD allele frequency 4.12e-1
rs1333049 is a genetic variant located in the CDKN2B-AS1 gene. dbsnp · gene
In gnomAD, rs1333049 has an overall allele frequency of 41.2%. gnomad · frequency
In ClinVar, rs1333049 is classified as Risk factor for Three Vessel Coronary Disease (0 review stars, somatic). clinvar · classificationclinvar · review confidenceclinvar · origin
retrieved 2026-08-03 · facts 483bbcf85d0c4590 · 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.