SERPINB13, serpin family B member 13, 5275

N. diseases: 5; N. variants: 2
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: rs12968338
rs12968338
Entrez Id: 5275
Gene Symbol: SERPINB13
SERPINB13
CUI: C0200638
Disease:
Eosinophil count procedure 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016