Gene: MYH6 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4624
Gene Symbol: MYH6
MYH6 		0.630 GeneticVariation disease BEFREE We screened 9 genotype-negative probands with sick sinus syndrome families for mutations in MYH6 and identified an in-frame 3-bp deletion predicted to delete one residue (delE933) at the highly conserved coiled-coil structure within the binding motif to myosin-binding protein C in one patient. 25717017 2015
Entrez Id: 4624
Gene Symbol: MYH6
MYH6 		0.630 GeneticVariation disease BEFREE MYH6 variants have been identified in patients with atrial septal defects, cardiomyopathies, and sick sinus syndrome. 26284702 2015
Entrez Id: 4624
Gene Symbol: MYH6
MYH6 		0.630 Biomarker disease CTD_human A rare variant in MYH6 is associated with high risk of sick sinus syndrome. 21378987 2011
Entrez Id: 4624
Gene Symbol: MYH6
MYH6 		0.630 GeneticVariation disease BEFREE A rare variant in MYH6 is associated with high risk of sick sinus syndrome. 21378987 2011
Entrez Id: 4624
Gene Symbol: MYH6
MYH6 		0.630 GeneticVariation disease GWASDB A rare variant in MYH6 is associated with high risk of sick sinus syndrome. 21378987 2011
Entrez Id: 4624
Gene Symbol: MYH6
MYH6 		0.630 SusceptibilityMutation disease ORPHANET