Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8177318
rs8177318
Entrez Id: 7018;100129696
Gene Symbol: TF;INHCAP
TF;INHCAP
CUI: C0427460
Disease:
Red cell distribution width determination
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016