SLC22A4, solute carrier family 22 member 4, 6583

N. diseases: 90; N. variants: 21
Disease: Eosinophil count procedure ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10075801
rs10075801
Entrez Id: 6583;553103
Gene Symbol: SLC22A4;MIR3936HG
SLC22A4;MIR3936HG
CUI: C0200638
Disease:
Eosinophil count procedure 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016