rs10738604 - CDKN2B-AS1

Magnitude 2.2 · 1 study on file

Reported associations

• Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure - Unknown journal (n.d.) · Unknown authors · PubMed 36376295

  ABSTRACT: Heart failure is a leading cause of cardiovascular morbidity and mortality. However, the contribution of common genetic variation to heart failure risk has not been fully elucidated, particularly in comparison to other common cardiometabolic traits. We report a multi-ancestry genome-wide association study meta-analysis of all-cause heart failure including up to 115,150 cases and 1,550,331 controls of diverse genetic ancestry, identifying 47 risk loci. We also perform multivariate genome-wide association studies that integrate heart failure with related cardiac magnetic resonance imaging endophenotypes, identifying 61 risk loci. Gene-prioritization analyses including colocalization and transcriptome-wide association studies identify known and previously unreported candidate cardio

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