ISG15, ISG15 ubiquitin like modifier, 9636

N. diseases: 7; N. variants: 5
Source: CURATED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1891906
rs1891906
Entrez Id: 9636
Gene Symbol: ISG15
ISG15
CUI: C2985280
Disease:
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs3121567
rs3121567
Entrez Id: 9636
Gene Symbol: ISG15
ISG15
CUI: C2985280
Disease:
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
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