Disease: Monocyte count procedure ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34557412
rs34557412
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0200637
Disease:
Monocyte count procedure 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016