Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852890
rs137852890
GBE1
CUI: C1856304
Disease: GSD IV, Neuromuscular Form, Congenital
GSD IV, Neuromuscular Form, Congenital 		A 0.700 CausalMutation CLINVAR

dbSNP: rs137852892
rs137852892
GBE1
CUI: C1856304
Disease: GSD IV, Neuromuscular Form, Congenital
GSD IV, Neuromuscular Form, Congenital 		G 0.700 CausalMutation CLINVAR

dbSNP: rs137852893
rs137852893
GBE1
CUI: C1856304
Disease: GSD IV, Neuromuscular Form, Congenital
GSD IV, Neuromuscular Form, Congenital 		A 0.700 CausalMutation CLINVAR

dbSNP: rs137852894
rs137852894
GBE1
CUI: C1856304
Disease: GSD IV, Neuromuscular Form, Congenital
GSD IV, Neuromuscular Form, Congenital 		T 0.700 CausalMutation CLINVAR

dbSNP: rs397515342
rs397515342
GBE1
CUI: C1856304
Disease: GSD IV, Neuromuscular Form, Congenital
GSD IV, Neuromuscular Form, Congenital 		T 0.700 CausalMutation CLINVAR

dbSNP: rs397515344
rs397515344
GBE1
CUI: C1856304
Disease: GSD IV, Neuromuscular Form, Congenital
GSD IV, Neuromuscular Form, Congenital 		G 0.700 CausalMutation CLINVAR