Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs797044938
rs797044938
KCNQ2
CUI: C0036572
Disease: Seizures
Seizures 		A 0.700 CausalMutation CLINVAR Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy. 26795593

2016
dbSNP: rs797044938
rs797044938
KCNQ2
CUI: C0036572
Disease: Seizures
Seizures 		A 0.700 GeneticVariation CLINVAR