Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs377079849
rs377079849
Entrez Id: 1107;84316
Gene Symbol: CHD3;NAA38
CHD3;NAA38
CUI: C0857490
Disease:
Granulocyte count
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016