SLC16A9, solute carrier family 16 member 9, 220963

N. diseases: 12; N. variants: 32
Disease: Acylcarnitines measurement ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1171606
rs1171606
Entrez Id: 220963
Gene Symbol: SLC16A9
SLC16A9
CUI: C0523446
Disease:
Acylcarnitines measurement 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. 26068415 2015
dbSNP: rs1171614
rs1171614
Entrez Id: 220963
Gene Symbol: SLC16A9
SLC16A9
CUI: C0523446
Disease:
Acylcarnitines measurement 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. 26068415 2015
dbSNP: rs1171616
rs1171616
Entrez Id: 220963
Gene Symbol: SLC16A9
SLC16A9
CUI: C0523446
Disease:
Acylcarnitines measurement 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. 26068415 2015