rs114241858 - LINC03079 - LINC00494
Magnitude 4.5 · 1 study on file
Reported associations
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A Genome-Wide Association Study of Idiopathic Dilated Cardiomyopathy in African Americans - Unknown journal (n.d.) · Unknown authors · PubMed 29495422
ABSTRACT: Idiopathic dilated cardiomyopathy (IDC) is the most common form of non-ischemic chronic heart failure. Despite the higher prevalence of IDC in African Americans, the genetics of IDC have been relatively understudied in this ethnic group. We performed a genome-wide association study to identify susceptibility genes for IDC in African Americans recruited from five sites in the U.S. (662 unrelated cases and 1167 controls). The heritability of IDC was calculated to be 33% (95% confidence interval: 19-47%; p = 6.4 × 10−7). We detected association of a variant in a novel intronic locus in the CACNB4 gene meeting genome-wide levels of significance (p = 4.1 × 10−8). The CACNB4 gene encodes a calcium channel subunit expressed in the heart that is important for cardiac muscle contr
Auto-generated from study metadata. AI-synthesised commentary is added when this entry is regenerated through content-service's LLM mode.
Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Discuss with your doctor
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genetic risk for dilated cardiomyopathy Moderate
rs114241858-C allele associates with 1.71-fold increased risk of idiopathic dilated cardiomyopathy
consult cardiologist for risk evaluation and screening plan
Screening
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echocardiography for left ventricular function Moderate
genetic predisposition to DCM warrants baseline cardiac imaging
obtain baseline echocardiography
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heart failure symptoms Moderate
increased genetic risk warrants heightened awareness of DCM symptoms
be alert to shortness of breath, palpitations, chest pain, fatigue