rs137854600, SCN5A

N. diseases: 6
Disease: Ventricular arrhythmia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Ventricular arrhythmia
CUI: C0085612
Disease: Ventricular arrhythmia
0.010 GeneticVariation BEFREE The surviving infant was found to have a heterozygous mutation in SCN5A (R1623Q), previously reported as a de novo mutation causing neonatal ventricular arrhythmia and LQTS. 15184283 2004