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Article

A common variant at 9p21 is associated with sudden and arrhythmic cardiac death.

Circulation - 24 Nov 2009

Newton-Cheh Christopher, Cook Nancy R, VanDenburgh Martin, Rimm Eric B, Ridker Paul M, Albert Christine M

Abstract excerpt

BACKGROUND: Although a heritable basis for sudden cardiac death (SCD) is suggested by the impact of family history on SCD risk, common genetic determinants have been difficult to identify. We hypothesized that a common variant at chromosome 9p21 related to myocardial infarction would influence SC...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 9

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Share to Polymorphism, Single Nucleotide

Source

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Identifiers

PMID: 19901189
DOI: 10.1161/CIRCULATIONAHA.109.879049
PMCID: PMC2785227

Genes

SCD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19901189-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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