SLC16A9, solute carrier family 16 member 9, 220963

N. diseases: 12; N. variants: 32
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: rs1171616
rs1171616
Entrez Id: 220963
Gene Symbol: SLC16A9
SLC16A9
CUI: C0022661
Disease:
Kidney Failure, Chronic 		T 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352 2018