MYO1D, myosin ID, 4642

N. diseases: 16; N. variants: 11
Disease: Reticulocyte count (procedure) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17780981
rs17780981
Entrez Id: 4642
Gene Symbol: MYO1D
MYO1D
CUI: C0206161
Disease:
Reticulocyte count (procedure) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016