Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 3 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587780450
rs587780450
Entrez Id: 6326
Gene Symbol: SCN2A
SCN2A
CUI: C1843140
Disease:
SEIZURES, BENIGN FAMILIAL INFANTILE, 3 		G 0.700 CausalMutation CLINVAR