Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs794726778
rs794726778
SCN1A ; SCN1A-AS1
A 0.700 CausalMutation CLINVAR Seven novel SCN1A mutations in Chinese patients with severe myoclonic epilepsy of infancy. 18554359

2008