SFXN2, sideroflexin 2, 118980

N. diseases: 5; N. variants: 3
Disease: White Blood Cell Count procedure ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7917772
rs7917772
Entrez Id: 118980
Gene Symbol: SFXN2
SFXN2
CUI: C0023508
Disease:
White Blood Cell Count procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016