TTN-AS1, TTN antisense RNA 1, 100506866

N. diseases: 78; N. variants: 567
Source: CLINVAR ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.100 GeneticVariation disease CLINVAR
CUI: C0023212
Disease: Left-Sided Heart Failure
Left-Sided Heart Failure 		0.100 CausalMutation disease CLINVAR
CUI: C0023212
Disease: Left-Sided Heart Failure
Left-Sided Heart Failure 		0.100 GeneticVariation disease CLINVAR
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.100 GeneticVariation disease CLINVAR
CUI: C0027092
Disease: Myopia
Myopia 		0.100 GeneticVariation disease CLINVAR
CUI: C0027092
Disease: Myopia
Myopia 		0.100 CausalMutation disease CLINVAR
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		0.100 GeneticVariation disease CLINVAR
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome 		0.100 GeneticVariation disease CLINVAR
CUI: C0079352
Disease: Congenital torticollis
Congenital torticollis 		0.100 CausalMutation disease CLINVAR
CUI: C0079352
Disease: Congenital torticollis
Congenital torticollis 		0.100 GeneticVariation disease CLINVAR
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia 		0.100 GeneticVariation disease CLINVAR
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block 		0.100 GeneticVariation disease CLINVAR
CUI: C0175709
Disease: Centronuclear myopathy
Centronuclear myopathy 		0.100 GeneticVariation disease CLINVAR Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease. 25589632 2015
CUI: C0175709
Disease: Centronuclear myopathy
Centronuclear myopathy 		0.100 GeneticVariation disease CLINVAR Truncations of titin causing dilated cardiomyopathy. 22335739 2012
CUI: C0221217
Disease: Neck webbing
Neck webbing 		0.100 CausalMutation disease CLINVAR
CUI: C0221217
Disease: Neck webbing
Neck webbing 		0.100 GeneticVariation disease CLINVAR
CUI: C0281788
Disease: Biventricular hypertrophy
Biventricular hypertrophy 		0.100 GeneticVariation disease CLINVAR
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		0.100 CausalMutation disease CLINVAR
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		0.100 GeneticVariation disease CLINVAR
CUI: C0340477
Disease: Re-entrant atrioventricular tachycardia
Re-entrant atrioventricular tachycardia 		0.100 GeneticVariation disease CLINVAR
CUI: C0340477
Disease: Re-entrant atrioventricular tachycardia
Re-entrant atrioventricular tachycardia 		0.100 CausalMutation disease CLINVAR
CUI: C0699743
Disease: Congenital muscular dystrophy (disorder)
Congenital muscular dystrophy (disorder) 		0.100 GeneticVariation disease CLINVAR
CUI: C0702166
Disease: Acne
Acne 		0.100 GeneticVariation disease CLINVAR
CUI: C0702166
Disease: Acne
Acne 		0.100 CausalMutation disease CLINVAR
CUI: C0749379
Disease: Thoracolumbar scoliosis
Thoracolumbar scoliosis 		0.100 GeneticVariation disease CLINVAR