NECTIN2, LNCOB1 NECTIN2, LNCOB1
NECTIN2, LNCOB1 (NECTIN2, LNCOB1): 6 variants described, covering trait, health risk.
Which NECTIN2, LNCOB1 variants does Orviva describe?
- rs12972970 Trait imported
- G allele associated with decreased risk of Metabolic syndrome (OR=0.13). [GWAS Catalog]
- rs283814 Health risk imported
- G allele associated with increased Triglyceride levels (β=0.060). [GWAS Catalog]
- rs283815 Health risk imported
- A allele associated with increased Triglycerides x depression interaction (2df test) (β=0.005). [GWAS Catalog]
- rs34342646 Trait imported
- G allele associated with decreased risk of Metabolic syndrome (OR=0.13). [GWAS Catalog]
2 further NECTIN2, LNCOB1 variants in the knowledge base have only a brief annotation and are not listed here.
See your own NECTIN2, LNCOB1 genotypes
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my NECTIN2, LNCOB1 variants say about me?”
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my NECTIN2, LNCOB1 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.