Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8557
Gene Symbol: TCAP
TCAP 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 4563
Gene Symbol: TRNG
TRNG 		0.100 CausalMutation disease CLINVAR
Entrez Id: 4565
Gene Symbol: TRNI
TRNI 		0.100 CausalMutation disease CLINVAR
Entrez Id: 1674
Gene Symbol: DES
DES 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 2717
Gene Symbol: GLA
GLA 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 8557
Gene Symbol: TCAP
TCAP 		0.100 CausalMutation disease CLINVAR
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 2273
Gene Symbol: FHL1
FHL1 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 100529097
Gene Symbol: RPL36A-HNRNPH2
RPL36A-HNRNPH2 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations. 1430197 1992
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations. 1430197 1992
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. 1552912 1992
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the beta-myosin heavy chain gene. A 908Leu----Val mutation and a 403Arg----Gln mutation. 1638703 1992
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes. 1944483 1991
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation. 1975517 1990
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR [Biochemical characterization of a high-molecular weight alkaline phosphatase in a patient with cholangiocarcinoma (alpha-1 alkaline phosphatase)]. 2411171 1985
Entrez Id: 4607
Gene Symbol: MYBPC3
MYBPC3 		0.500 CausalMutation disease CLINVAR Development of an osteogenic bone-marrow preparation. 2732257 1989
Entrez Id: 4607
Gene Symbol: MYBPC3
MYBPC3 		0.500 CausalMutation disease CLINVAR Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. 7493025 1995
Entrez Id: 4607
Gene Symbol: MYBPC3
MYBPC3 		0.500 CausalMutation disease CLINVAR Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy. 7493026 1995
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 GeneticVariation disease CLINVAR Recent advances in the molecular genetics of hypertrophic cardiomyopathy. 7648684 1995
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutations. 7662452 1995
Entrez Id: 7168
Gene Symbol: TPM1
TPM1 		0.500 CausalMutation disease CLINVAR A de novo mutation in alpha-tropomyosin that causes hypertrophic cardiomyopathy. 7729014 1995
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy. 7731997 1995
Entrez Id: 4607
Gene Symbol: MYBPC3
MYBPC3 		0.500 Biomarker disease BEFREE The gene coding for cardiac MyBP-C has been assigned to the chromosomal location 11p11.2 in humans, and is therefore in a region of physical linkage to subsets of familial hypertrophic cardiomyopathy (FHC). 7744002 1995
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.500 CausalMutation disease CLINVAR A myosin missense mutation, not a null allele, causes familial hypertrophic cardiomyopathy. 7796500 1995