LNCRNA-IUR - FAM76B LNCRNA-IUR - FAM76B
LNCRNA-IUR - FAM76B (LNCRNA-IUR - FAM76B): 33 variants described, covering trait, health risk, nutrition.
Which LNCRNA-IUR - FAM76B variants does Orviva describe?
- rs11021232 Health risk imported
- C allele associated with slightly increased risk of Vitiligo (OR=1.33). [GWAS Catalog]
- rs12575636 Health risk imported
- T allele associated with increased Sex hormone-binding globulin levels adjusted for BMI (β=0.010). [GWAS Catalog]
31 further LNCRNA-IUR - FAM76B variants in the knowledge base have only a brief annotation and are not listed here.
See your own LNCRNA-IUR - FAM76B genotypes
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my LNCRNA-IUR - FAM76B variants say about me?”
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my LNCRNA-IUR - FAM76B 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.