Gene: MYH7 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913647
rs121913647
MYH7 ; MHRT
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555338080
rs1555338080
MYH7
G 0.700 GeneticVariation CLINVAR

dbSNP: rs377491278
rs377491278
MYH7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs397516122
rs397516122
MYH7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs397516123
rs397516123
MYH7
A 0.700 GeneticVariation CLINVAR

dbSNP: rs397516224
rs397516224
MYH7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs397516252
rs397516252
MYH7 ; MHRT
C 0.700 GeneticVariation CLINVAR

dbSNP: rs397516253
rs397516253
MYH7 ; MHRT
G 0.700 GeneticVariation CLINVAR

dbSNP: rs45516091
rs45516091
MYH7
A 0.700 GeneticVariation CLINVAR

dbSNP: rs727503265
rs727503265
MYH7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs760187215
rs760187215
MYH7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs869025483
rs869025483
MYH7 ; MHRT
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121913642
rs121913642
MYH7
G 0.700 CausalMutation CLINVAR Human growth hormone stimulates somatomedin C/insulin-like growth factor I production by the human lymphoid cell line, IM-9. 2753225

1989
dbSNP: rs121913642
rs121913642
MYH7
G 0.700 CausalMutation CLINVAR Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy. 11106718

2000
dbSNP: rs45544633
rs45544633
MYH7 ; MHRT
A 0.700 GeneticVariation CLINVAR Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy. 15556047

2004
dbSNP: rs397516258
rs397516258
MYH7
G 0.700 GeneticVariation CLINVAR Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene. 15769782

2005
dbSNP: rs121913642
rs121913642
MYH7
G 0.700 CausalMutation CLINVAR Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function. 16983074

2006
dbSNP: rs121913642
rs121913642
MYH7
G 0.700 CausalMutation CLINVAR Hypertrophic and dilated cardiomyopathy mutations differentially affect the molecular force generation of mouse alpha-cardiac myosin in the laser trap assay. 17351073

2007
dbSNP: rs45544633
rs45544633
MYH7 ; MHRT
A 0.700 GeneticVariation CLINVAR Cardiac magnetic resonance imaging of myocardial contrast uptake and blood flow in patients affected with idiopathic or familial dilated cardiomyopathy. 18660445

2008
dbSNP: rs45516091
rs45516091
MYH7
A 0.700 CausalMutation CLINVAR Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy. 19412328

2008
dbSNP: rs45544633
rs45544633
MYH7 ; MHRT
A 0.700 GeneticVariation CLINVAR Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy. 19412328

2008
dbSNP: rs397516248
rs397516248
MYH7 ; MHRT
T 0.700 GeneticVariation CLINVAR 165th ENMC International Workshop: distal myopathies 6-8th February 2009 Naarden, The Netherlands. 19477645

2009
dbSNP: rs397516248
rs397516248
MYH7 ; MHRT
T 0.700 CausalMutation CLINVAR 165th ENMC International Workshop: distal myopathies 6-8th February 2009 Naarden, The Netherlands. 19477645

2009
dbSNP: rs45544633
rs45544633
MYH7 ; MHRT
A 0.700 GeneticVariation CLINVAR Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes. 19854198

2010
dbSNP: rs397516089
rs397516089
MYH7
T 0.700 CausalMutation CLINVAR Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation. 20031619

2009