9p21.3/CDKN2A/B 9p21.3 locus near CDKN2A/CDKN2B
9p21.3/CDKN2A/B (9p21.3 locus near CDKN2A/CDKN2B): 1 variant described, covering health risk.
Which 9p21.3/CDKN2A/B variants does Orviva describe?
- rs1333049 Health risk
- Significantly increased risk for coronary artery disease. 9p21.3 is the strongest known genetic risk factor for CAD.
See your own 9p21.3/CDKN2A/B genotypes
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my 9p21.3/CDKN2A/B variants say about me?”
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my 9p21.3/CDKN2A/B variants say about me?”
Genetic associations describe risk across populations, not a diagnosis for any one person. Most variants shift risk modestly and act alongside lifestyle, environment and other genes. Consumer DNA chips do not read every position and can be wrong at any single one. For general education only; talk to a clinician or genetic counsellor before acting on anything here, and never change a prescribed medicine without your prescriber.