HLX, H2.0 like homeobox, 3142

N. diseases: 28; N. variants: 6
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: rs41369048
rs41369048
Entrez Id: 3142;100873924
Gene Symbol: HLX;HLX-AS1
HLX;HLX-AS1
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