Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs115340020
rs115340020
Entrez Id: 11146;79871
Gene Symbol: GLMN;RPAP2
GLMN;RPAP2
CUI: C0200637
Disease:
Monocyte count procedure
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016