SNX13 SNX13
SNX13 (SNX13): 18 variants described, covering health risk, nutrition, trait.
Which SNX13 variants does Orviva describe?
- rs10242866 Health risk imported
- C allele associated with increased Height (β=0.011). [GWAS Catalog]
- rs17138358 Nutrition imported
- G allele associated with increased HDL cholesterol levels (β=0.027). [GWAS Catalog]
- rs1917368 Nutrition imported
- G allele associated with increased high density lipoprotein cholesterol (HDLC, mean, inv-norm transformed) (β=0.045). [GWAS Catalog]
15 further SNX13 variants in the knowledge base have only a brief annotation and are not listed here.
See your own SNX13 genotypes
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my SNX13 variants say about me?”
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my SNX13 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.