BCL2L13, BCL2 like 13, 23786

N. diseases: 18; 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: rs4819618
rs4819618
Entrez Id: 23786
Gene Symbol: BCL2L13
BCL2L13
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs34891900
rs34891900
Entrez Id: 23786
Gene Symbol: BCL2L13
BCL2L13
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