Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4653
Gene Symbol: MYOC
MYOC
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.150 GeneticVariation BEFREE To investigate the association between high myopia (HM) and single nucleotide polymorphisms (SNPs) in the myocilin (MYOC), hepatocyte growth factor (HGF), hepatocyte growth factor receptor (MET), and aggrecan (ACAN) genes in a Han Chinese population. 24766640

2014
Entrez Id: 4653
Gene Symbol: MYOC
MYOC
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.150 Biomarker BEFREE Our results confirm that the PAX6, Lumican, and MYOC genes were not associated with high myopia in the Han Chinese in Northeastern China. 22809227

2012
Entrez Id: 4653
Gene Symbol: MYOC
MYOC
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.150 Biomarker BEFREE Myocilin seems to be a very strong candidate for explaining some of the pathophysiological pathways leading to the development of both glaucoma and high myopia. 19260140

2009
Entrez Id: 4653
Gene Symbol: MYOC
MYOC
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.150 Biomarker BEFREE Association between high myopia and MYOC polymorphisms was assessed using the Unphased program. 19180258

2009
Entrez Id: 4653
Gene Symbol: MYOC
MYOC
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.150 GeneticVariation BEFREE Linkage and association of myocilin (MYOC) polymorphisms with high myopia in a Chinese population. 17438518

2007