rs773724817, KCNH2

N. diseases: 4
Disease: Epilepsy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.010 GeneticVariation BEFREE R863X alteration in HERG channel may be involved in both prolonged QTc interval and epilepsy. 22515331 2012