MYO1D, myosin ID, 4642

N. diseases: 16; N. variants: 11
Disease: Refractive Errors ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17183295
rs17183295
Entrez Id: 4642
Gene Symbol: MYO1D
MYO1D
CUI: C0034951
Disease:
Refractive Errors 		T 0.700 GeneticVariation GWASDB Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134 2013