The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study.

doi:10.1093/eurheartj/ehl460

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Article

The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study.

European heart journal - 1 Feb 2007

Akyol Mahmut, Jalilzadeh Shapour, Sinner Moritz F, Perz Siegfried, Beckmann Britt M, Gieger Christian, Illig Thomas, Wichmann H-Erich, Meitinger Thomas, Kääb Stefan, Pfeufer Arne

Abstract excerpt

AIMS: The QT interval in the general population is a complex trait with 30-50% heritability. QT prolongation is associated with an increased risk of sudden death. A recent family-based study found an association between QT interval and the common non-synonymous Glycin 38 Serine variant (G38S, rs1...

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PMID: 17227789
DOI: 10.1093/eurheartj/ehl460

Genes

KCNH2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17227789-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study.PMID 17227789Read ↗

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