rs12047439 - SCMH1-DT - FOXO6

Magnitude 2.2 · 1 study on file

Reported associations

  • Large-scale genome-wide association study of coronary artery disease in genetically diverse populations - Unknown journal (n.d.) · Unknown authors · PubMed 35915156

    ABSTRACT: We report a genome-wide association study (GWAS) of coronary artery disease (CAD) incorporating nearly a quarter million cases, in which existing studies are integrated with data from cohorts of White, Black, and Hispanic individuals from the Million Veteran Program. We document near equivalent heritability of CAD across multiple ancestral groups, identify 95 novel loci, including the first nine to be identified on the X-chromosome, detect the first eight genome-wide significant loci among Blacks and Hispanics, and demonstrate that two common haplotypes at the 9p21 locus are responsible for risk stratification in all populations except those of African origin, where these haplotypes are virtually absent. Moreover, in the largest GWAS for angiographically derived coronary atherosc


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Lifestyle context

Concrete actions anchored to the cited research. We do not prescribe, we describe.

Screening

  • earlier coronary artery disease screening Moderate

    Genetic variant associated with coronary artery disease risk and altered SCMH1-DT and FOXO6 expression in cardiac and metabolic tissues

    Discuss with primary care about earlier CAD screening based on genetic risk, typically starting in 30s-40s