Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7273
Gene Symbol: TTN
TTN 		0.640 CausalMutation disease CLINVAR
Entrez Id: 7273
Gene Symbol: TTN
TTN 		0.640 GeneticVariation disease CLINVAR
Entrez Id: 282996
Gene Symbol: RBM20
RBM20 		0.450 GeneticVariation disease CLINVAR
Entrez Id: 9531
Gene Symbol: BAG3
BAG3 		0.430 GeneticVariation disease CLINVAR
Entrez Id: 9531
Gene Symbol: BAG3
BAG3 		0.430 CausalMutation disease CLINVAR
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2 		0.430 GeneticVariation disease CLINVAR
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.430 CausalMutation disease CLINVAR
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.410 CausalMutation disease CLINVAR
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.410 GeneticVariation disease CLINVAR
Entrez Id: 4624
Gene Symbol: MYH6
MYH6 		0.400 CausalMutation disease CLINVAR
Entrez Id: 4607
Gene Symbol: MYBPC3
MYBPC3 		0.400 CausalMutation disease CLINVAR
Entrez Id: 4607
Gene Symbol: MYBPC3
MYBPC3 		0.400 GeneticVariation disease CLINVAR
Entrez Id: 4000
Gene Symbol: LMNA
LMNA 		0.200 CausalMutation disease CLINVAR
Entrez Id: 100506866
Gene Symbol: TTN-AS1
TTN-AS1 		0.100 CausalMutation disease CLINVAR
Entrez Id: 100506866
Gene Symbol: TTN-AS1
TTN-AS1 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 4000
Gene Symbol: LMNA
LMNA 		0.200 GeneticVariation disease BEFREE Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations. 15219508 2004
Entrez Id: 1756
Gene Symbol: DMD
DMD 		0.340 GeneticVariation disease BEFREE Familial dilated cardiomyopathy secondary to dystrophin splice site mutation. 20206892 2010
Entrez Id: 4000
Gene Symbol: LMNA
LMNA 		0.200 GeneticVariation disease BEFREE Familial dilated cardiomyopathy with conduction system defects variably associated with skeletal muscle abnormalities is frequently caused by LMNA gene mutations. 21462202 2011
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.410 GeneticVariation disease BEFREE MYH7 appears as the most frequently mutated gene in our FDCM population (approximately 10%), and mutation carriers present with delayed onset, in contrast to TNNT2. 15769782 2005
Entrez Id: 4000
Gene Symbol: LMNA
LMNA 		0.200 Biomarker disease BEFREE Lamin A/C deficiency is probably the most common cause of familial dilated cardiomyopathy. 19384091 2009
Entrez Id: 2697
Gene Symbol: GJA1
GJA1 		0.010 GeneticVariation disease BEFREE Connexin 43 remodeling induced by LMNA gene mutation Glu82Lys in familial dilated cardiomyopathy with atrial ventricular block. 20497714 2010
Entrez Id: 2626
Gene Symbol: GATA4
GATA4 		0.020 GeneticVariation disease BEFREE GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy. 24041700 2013
Entrez Id: 2627
Gene Symbol: GATA6
GATA6 		0.010 GeneticVariation disease BEFREE GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy. 25119427 2014
Entrez Id: 140628
Gene Symbol: GATA5
GATA5 		0.010 GeneticVariation disease BEFREE GATA5 loss-of-function mutation in familial dilated cardiomyopathy. 25543888 2015
Entrez Id: 54897
Gene Symbol: CASZ1
CASZ1 		0.010 GeneticVariation disease BEFREE CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy. 28099117 2017