MYO10, myosin X, 4651

N. diseases: 34; N. variants: 9
Disease: Cholecystolithiasis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs253314
rs253314
Entrez Id: 4651
Gene Symbol: MYO10
MYO10
CUI: C0947622
Disease:
Cholecystolithiasis 		0.700 GeneticVariation GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007