MedPage Today (5/29, Lou) reports, “Large-scale genetic testing turned up pathogenic variants for inherited cardiomyopathies in a meaningful proportion of the general population – especially among certain racial groups.” MedPage Today adds, “A 0.7% prevalence of known-pathogenic or likely pathogenic variants in cardiomyopathy genes was detected for men and women alike in the large nationwide All of Us cohort.” The data indicated that “the prevalence of these variants was 1.2% among people with South Asian ancestry, 0.8% both with European and with African ancestry, and 0.5% with East Asian ancestry.” The “carriers of these variants were at greater risk than non-carriers of developing the following: Heart failure: 3.05 vs 1.37 per 1,000 person-years (adjusted HR 2.30, 95% CI 2.04-2.60); Cardiomyopathy: 2.38 vs 0.54 per 1,000 person-years (aHR 4.31, 95% CI 3.73-4.97); Arrhythmia: 3.93 vs 2.09 per 1,000 person-years (aHR 2.12, 95% CI 1.78-2.53).” The findings were published in Circulation: Genomic and Precision Medicine.