TPCN2 - SMIM38 TPCN2 - SMIM38
TPCN2 - SMIM38 (TPCN2 - SMIM38): 4 variants described, covering trait, health risk.
Which TPCN2 - SMIM38 variants does Orviva describe?
- rs72932523 Health risk imported
- G allele associated with decreased risk of Blond vs. brown/black hair color (OR=0.45). [GWAS Catalog]
3 further TPCN2 - SMIM38 variants in the knowledge base have only a brief annotation and are not listed here.
See your own TPCN2 - SMIM38 genotypes
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my TPCN2 - SMIM38 variants say about me?”
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my TPCN2 - SMIM38 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.