KCTD16 - RN7SKP246 KCTD16 - RN7SKP246
KCTD16 - RN7SKP246 (KCTD16 - RN7SKP246): 5 variants described, covering trait, nutrition, health risk.
Which KCTD16 - RN7SKP246 variants does Orviva describe?
- rs463245 Health risk imported
- T allele associated with increased Insomnia (β=0.006). [GWAS Catalog]
4 further KCTD16 - RN7SKP246 variants in the knowledge base have only a brief annotation and are not listed here.
See your own KCTD16 - RN7SKP246 genotypes
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my KCTD16 - RN7SKP246 variants say about me?”
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my KCTD16 - RN7SKP246 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.