rs1805127, KCNE1

N. diseases: 17
Disease: Long QT Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Long QT Syndrome
CUI: C0023976
Disease: Long QT Syndrome
0.020 GeneticVariation BEFREE Although KCNE1(G38S), a single-nucleotide polymorphism (SNP) causing a G38S substitution in KCNE1, is found frequently, whether and how this SNP causes long QT syndrome (LQTS) remains unclear. 27255646 2017
Long QT Syndrome
CUI: C0023976
Disease: Long QT Syndrome
0.020 GeneticVariation BEFREE Patients with KCNE1(G38S) could have similar potential risk of ventricular arrhythmia as with LQTS. 26520166 2016