MYH7B, myosin heavy chain 7B, 57644

N. diseases: 18; N. variants: 20
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0919677
Disease: Protein C measurement
Protein C measurement
0.100 GeneticVariation phenotype GWASCAT Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project. 22443383 2012
CUI: C0919677
Disease: Protein C measurement
Protein C measurement
0.100 GeneticVariation phenotype GWASDB Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project. 22443383 2012
CUI: C0919677
Disease: Protein C measurement
Protein C measurement
0.100 GeneticVariation phenotype GWASDB A genome-wide association study of the Protein C anticoagulant pathway. 22216198 2011
CUI: C0919677
Disease: Protein C measurement
Protein C measurement
0.100 GeneticVariation phenotype GWASCAT A genome-wide association study of the Protein C anticoagulant pathway. 22216198 2011
CUI: C0919677
Disease: Protein C measurement
Protein C measurement
0.100 GeneticVariation phenotype GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010