KCNT2 - CFH KCNT2 - CFH
KCNT2 - CFH (KCNT2 - CFH): 5 variants described, covering trait, health risk.
Which KCNT2 - CFH variants does Orviva describe?
- rs3043084 Health risk imported
- A allele associated with decreased risk of Macular degeneration, dry (PheCode 362.21) (OR=0.59). [GWAS Catalog]
4 further KCNT2 - CFH variants in the knowledge base have only a brief annotation and are not listed here.
See your own KCNT2 - CFH genotypes
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my KCNT2 - CFH variants say about me?”
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my KCNT2 - CFH 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.