Disease: SEIZURES, BENIGN FAMILIAL INFANTILE, 2 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1301400509
rs1301400509
Entrez Id: 79447;112476
Gene Symbol: PAGR1;PRRT2
PAGR1;PRRT2
CUI: C1853995
Disease:
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 		T 0.700 CausalMutation CLINVAR