rs199472716, KCNQ1

N. diseases: 1
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
0.010 GeneticVariation BEFREE Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome. 12710526 2003