SNX11 SNX11
SNX11 (SNX11): 5 variants described, covering health risk, trait.
Which SNX11 variants does Orviva describe?
- rs10775406 Health risk imported
- A allele associated with increased triglyceride (mean, inv-norm transformed) (β=0.029). [GWAS Catalog]
4 further SNX11 variants in the knowledge base have only a brief annotation and are not listed here.
See your own SNX11 genotypes
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my SNX11 variants say about me?”
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my SNX11 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.