CTTNBP2 CTTNBP2
CTTNBP2 (CTTNBP2): 8 variants described, covering trait, health risk.
Which CTTNBP2 variants does Orviva describe?
- rs13239186 Health risk imported
- C allele associated with increased Noncognitive aspects of educational attainment (β=0.046). [GWAS Catalog]
- rs7795873 Trait imported
- T allele associated with increased Smoking cessation (MTAG) (β=0.012). [GWAS Catalog]
6 further CTTNBP2 variants in the knowledge base have only a brief annotation and are not listed here.
See your own CTTNBP2 genotypes
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my CTTNBP2 variants say about me?”
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my CTTNBP2 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.