ARG1, arginase 1, 383

N. diseases: 273; N. variants: 47
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28941474
rs28941474
Entrez Id: 383
Gene Symbol: ARG1
ARG1
CUI: C0268548
Disease:
Hyperargininemia 		C 0.810 CausalMutation CLINVAR
dbSNP: rs104893943
rs104893943
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		T 0.800 CausalMutation CLINVAR
dbSNP: rs104893948
rs104893948
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		C 0.800 CausalMutation CLINVAR
dbSNP: rs104893942
rs104893942
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		G 0.700 CausalMutation CLINVAR
dbSNP: rs104893947
rs104893947
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		A 0.700 CausalMutation CLINVAR
dbSNP: rs113767658
rs113767658
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1169538148
rs1169538148
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554249332
rs1554249332
Entrez Id: 383
Gene Symbol: ARG1
ARG1
CUI: C0268548
Disease:
Hyperargininemia 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554250040
rs1554250040
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554251158
rs1554251158
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		GAAGA 0.700 GeneticVariation CLINVAR
dbSNP: rs1554251191
rs1554251191
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1554251356
rs1554251356
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1562356664
rs1562356664
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1562361837
rs1562361837
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		T 0.700 CausalMutation CLINVAR
dbSNP: rs747579073
rs747579073
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs755359126
rs755359126
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs776939220
rs776939220
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		AT 0.700 GeneticVariation CLINVAR
dbSNP: rs796051923
rs796051923
Entrez Id: 383;9439
Gene Symbol: ARG1;MED23
ARG1;MED23
CUI: C0268548
Disease:
Hyperargininemia 		CG 0.700 GeneticVariation CLINVAR
dbSNP: rs9375818
rs9375818
Entrez Id: 383
Gene Symbol: ARG1
ARG1
CUI: C0017654
Disease:
Glomerular Filtration Rate 		A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs2807278
rs2807278
Entrez Id: 383
Gene Symbol: ARG1
ARG1
CUI: C0028754
Disease:
Obesity 		0.800 GeneticVariation GWASDB A genome-wide association study on obesity and obesity-related traits. 21552555 2011
dbSNP: rs2807278
rs2807278
Entrez Id: 383
Gene Symbol: ARG1
ARG1
CUI: C0028754
Disease:
Obesity 		0.800 GeneticVariation GWASCAT A genome-wide association study on obesity and obesity-related traits. 21552555 2011
dbSNP: rs143633948
rs143633948
Entrez Id: 383
Gene Symbol: ARG1
ARG1
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 GeneticVariation GWASCAT A new 3p25 locus is associated with liver fibrosis progression in human immunodeficiency virus/hepatitis C virus-coinfected patients. 27339598 2016
dbSNP: rs143633948
rs143633948
Entrez Id: 383
Gene Symbol: ARG1
ARG1
CUI: C0019196
Disease:
Hepatitis C 		0.700 GeneticVariation GWASCAT A new 3p25 locus is associated with liver fibrosis progression in human immunodeficiency virus/hepatitis C virus-coinfected patients. 27339598 2016
dbSNP: rs143633948
rs143633948
Entrez Id: 383
Gene Symbol: ARG1
ARG1
CUI: C2363741
Disease:
HIV-1 infection 		0.700 GeneticVariation GWASCAT A new 3p25 locus is associated with liver fibrosis progression in human immunodeficiency virus/hepatitis C virus-coinfected patients. 27339598 2016
dbSNP: rs143633948
rs143633948
Entrez Id: 383
Gene Symbol: ARG1
ARG1
CUI: C1836233
Disease:
AIDS, PROGRESSION TO 		0.700 GeneticVariation GWASCAT A new 3p25 locus is associated with liver fibrosis progression in human immunodeficiency virus/hepatitis C virus-coinfected patients. 27339598 2016