Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121917981
rs121917981
SCN1A ; SCN1A-AS1 ; LOC102724058
C 0.700 CausalMutation CLINVAR Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome. 23895530

2013