Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2273799
rs2273799
Entrez Id: 4005;105376621
Gene Symbol: LMO2;LOC105376621
LMO2;LOC105376621
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016