Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9330813
rs9330813
Entrez Id: 7477
Gene Symbol: WNT7B
WNT7B
CUI: C0018935
Disease:
Hematocrit procedure
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016