Article

Validation of GWAS-Identified CDKN2A Variant rs10757278 in Cardiomyopathy Patients of Pakistani Cohort

2025-01-21

Abstract excerpt

Cardiomyopathies, a leading cause of heart failure and mortality worldwide, are a diverse group of heart muscle disorders, with dilated cardiomyopathy being the most prevalent subtype. Numerous genetic variants, identified through GWAS and candidate gene studies, are associated with cardiomyopathies. This study aimed to evaluate the association of the rs10757278 SNP polymorphism on chromosome 9p21.3 near the CDKN2...

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Literature Corpus work: 9b40318e-47b3-5808-a99e-9e23f635e465
DOI: 10.20944/preprints202501.1486.v1

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