MYO1D, myosin ID, 4642

N. diseases: 16; N. variants: 11
Disease: Finding of Mean Corpuscular Hemoglobin ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80212824
rs80212824
Entrez Id: 4642
Gene Symbol: MYO1D
MYO1D
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019