SLC7A9, solute carrier family 7 member 9, 11136

N. diseases: 48; N. variants: 39
Disease: Kidney Failure, Chronic ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12460876
rs12460876
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0022661
Disease:
Kidney Failure, Chronic 		C 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352 2018
dbSNP: rs35975406
rs35975406
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0022661
Disease:
Kidney Failure, Chronic 		C 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352 2018
dbSNP: rs7252778
rs7252778
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0022661
Disease:
Kidney Failure, Chronic 		C 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352 2018
dbSNP: rs12460876
rs12460876
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0022661
Disease:
Kidney Failure, Chronic 		C 0.700 GeneticVariation GWASCAT New loci associated with kidney function and chronic kidney disease. 20383146 2010