SLC7A9, solute carrier family 7 member 9, 11136

N. diseases: 48; N. variants: 39
Disease: Creatinine measurement, serum (procedure) ×
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: C0201976
Disease:
Creatinine measurement, serum (procedure) 		T 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199 2016
dbSNP: rs12460876
rs12460876
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure) 		C 0.700 GeneticVariation GWASCAT New loci associated with kidney function and chronic kidney disease. 20383146 2010