MYO1C, myosin IC, 4641

N. diseases: 29; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34582191
rs34582191
Entrez Id: 4641
Gene Symbol: MYO1C
MYO1C
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9905106
rs9905106
Entrez Id: 4641
Gene Symbol: MYO1C
MYO1C
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs8066044
rs8066044
Entrez Id: 4641
Gene Symbol: MYO1C
MYO1C
CUI: C0200638
Disease:
Eosinophil count procedure 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs8066044
rs8066044
Entrez Id: 4641
Gene Symbol: MYO1C
MYO1C
CUI: C0200633
Disease:
Neutrophil count (procedure) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016