ISG15, ISG15 ubiquitin like modifier, 9636

N. diseases: 7; N. variants: 5
Disease: IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION ×
Source: CURATED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs672601312
rs672601312
Entrez Id: 9636
Gene Symbol: ISG15
ISG15
CUI: C4015293
Disease:
IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION 		T 0.700 CausalMutation CLINVAR
dbSNP: rs672601345
rs672601345
Entrez Id: 9636
Gene Symbol: ISG15
ISG15
CUI: C4015293
Disease:
IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION 		CG 0.700 CausalMutation CLINVAR
dbSNP: rs786201005
rs786201005
Entrez Id: 9636
Gene Symbol: ISG15
ISG15
CUI: C4015293
Disease:
IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION 		T 0.700 CausalMutation CLINVAR