rs117067974, KCNQ2

N. diseases: 5
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Seizures
CUI: C0036572
Disease: Seizures
0.010 GeneticVariation BEFREE We hypothesize that patients with the KCNQ2 E515D mutation are susceptible to seizures. 28038823 2017