Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906281
rs387906281
Entrez Id: 85365
Gene Symbol: ALG2
ALG2
CUI: C1842836
Disease:
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii 		A 0.700 CausalMutation CLINVAR