SLC22A4, solute carrier family 22 member 4, 6583

N. diseases: 90; N. variants: 21
Disease: Acylcarnitines measurement ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs270601
rs270601
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
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