Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7273
Gene Symbol: TTN
TTN 		0.710 Biomarker disease GENOMICS_ENGLAND Congenital Titinopathy: Comprehensive characterization and pathogenic insights. 29691892 2018
Entrez Id: 7273
Gene Symbol: TTN
TTN 		0.710 Biomarker disease GENOMICS_ENGLAND A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population. 28295036 2017
Entrez Id: 7273
Gene Symbol: TTN
TTN 		0.710 Biomarker disease GENOMICS_ENGLAND Titin-truncating variants affect heart function in disease cohorts and the general population. 27869827 2017
Entrez Id: 7273
Gene Symbol: TTN
TTN 		0.710 CausalMutation disease CLINVAR Truncations of titin causing dilated cardiomyopathy. 22335739 2012
Entrez Id: 7273
Gene Symbol: TTN
TTN 		0.710 Biomarker disease GENOMICS_ENGLAND The genetics of dilated cardiomyopathy. 20186049 2010
Entrez Id: 7273
Gene Symbol: TTN
TTN 		0.710 GeneticVariation disease BEFREE C-terminal titin deletions cause a novel early-onset myopathy with fatal cardiomyopathy. 17444505 2007
Entrez Id: 7273
Gene Symbol: TTN
TTN 		0.710 GermlineCausalMutation disease ORPHANET C-terminal titin deletions cause a novel early-onset myopathy with fatal cardiomyopathy. 17444505 2007
Entrez Id: 7273
Gene Symbol: TTN
TTN 		0.710 Biomarker disease CTD_human
Entrez Id: 7273
Gene Symbol: TTN
TTN 		0.710 GeneticVariation disease CLINVAR
Entrez Id: 100506866
Gene Symbol: TTN-AS1
TTN-AS1 		0.100 CausalMutation disease CLINVAR Truncations of titin causing dilated cardiomyopathy. 22335739 2012
Entrez Id: 100506866
Gene Symbol: TTN-AS1
TTN-AS1 		0.100 GeneticVariation disease CLINVAR