Disease: Congenital Disorder Of Glycosylation, Type IIF ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554166294
rs1554166294
Entrez Id: 10559
Gene Symbol: SLC35A1
SLC35A1
CUI: C1970344
Disease:
Congenital Disorder Of Glycosylation, Type IIF 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1554166844
rs1554166844
Entrez Id: 10559
Gene Symbol: SLC35A1
SLC35A1
CUI: C1970344
Disease:
Congenital Disorder Of Glycosylation, Type IIF 		A 0.700 CausalMutation CLINVAR
dbSNP: rs578205635
rs578205635
Entrez Id: 10559
Gene Symbol: SLC35A1
SLC35A1
CUI: C1970344
Disease:
Congenital Disorder Of Glycosylation, Type IIF 		G 0.700 CausalMutation CLINVAR