LNCOB1, NECTIN2 LNCOB1, NECTIN2
LNCOB1, NECTIN2 (LNCOB1, NECTIN2): 7 variants described, covering trait, health risk.
Which LNCOB1, NECTIN2 variants does Orviva describe?
- rs12972156 Trait imported
- C allele associated with decreased risk of Metabolic syndrome (OR=0.13). [GWAS Catalog]
- rs6857 Trait imported
- T allele associated with moderately increased risk of Brain amyloid deposition (PET imaging) (OR=1.67). [GWAS Catalog]
5 further LNCOB1, NECTIN2 variants in the knowledge base have only a brief annotation and are not listed here.
See your own LNCOB1, NECTIN2 genotypes
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my LNCOB1, NECTIN2 variants say about me?”
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my LNCOB1, NECTIN2 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.