RN7SL513P - PGPEP1 RN7SL513P - PGPEP1
RN7SL513P - PGPEP1 (RN7SL513P - PGPEP1): 2 variants described, covering trait, health risk.
Which RN7SL513P - PGPEP1 variants does Orviva describe?
- rs9636202 Health risk imported
- G allele associated with marginally increased risk of Chronotype (OR=1.03). [GWAS Catalog]
1 further RN7SL513P - PGPEP1 variant in the knowledge base has only a brief annotation and is not listed here.
See your own RN7SL513P - PGPEP1 genotypes
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my RN7SL513P - PGPEP1 variants say about me?”
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my RN7SL513P - PGPEP1 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.