TNNT2

troponin T2, cardiac type
OMIM: 191045, ClinGen, DECIPHER

9 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 9 panels
Green TNNT2 in Dilated Cardiomyopathy Level 2: Cardiovascular disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, dilated, 1D, MIM# 601494
Green TNNT2 in Hypertrophic cardiomyopathy Level 2: Cardiovascular disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, hypertrophic, 2, MIM# 115195
Green TNNT2 in Incidentalome Version 1.0	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, dilated, 1D, MIM# 601494 Cardiomyopathy, hypertrophic, 2, MIM# 115195 Cardiomyopathy, familial restrictive, 3, MIM# 612422 Left ventricular noncompaction 6, MIM# 601494 Tags cardiac
Green TNNT2 in Additional findings_Adult Level 2: Screening Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance Phenotypes Cardiomyopathy, dilated, 1D, MIM# 601494 Cardiomyopathy, familial restrictive, 3, MIM# 612422 Cardiomyopathy, hypertrophic, 2, MIM# 115195 Left ventricular noncompaction 6, MIM# 601494
Green TNNT2 in Cardiomyopathy_Paediatric Level 2: Cardiovascular disorders Version 1.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green London South GLH South West GLH NHS GMS Phenotypes Cardiomyopathy, dilated, 1D Cardiomyopathy, familial hypertrophic, 2 Hypertrophic cardiomyopathy Left ventricular noncompaction 6,
Amber TNNT2 in Additional findings_Paediatric Level 2: Screening Version 1.0	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber BabySeq Category B gene Phenotypes Familial hypertrophic cardiomyopathy Cardiomyopathy, dilated
Red TNNT2 in Incidentalome_PREGEN_DRAFT Version 1.0	1 review	Unknown	Sources Expert Review Red NSW Health Pathology
Amber TNNT2 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 2.0	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category B gene Expert Review Amber Phenotypes Familial hypertrophic cardiomyopathy Cardiomyopathy, dilated
Green TNNT2 in Transplant Co-Morbidity Level 2: Screening Version 1.0	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, familial restrictive, 3, MIM# 612422 Cardiomyopathy, dilated, 1D, MIM# 601494 Left ventricular noncompaction 6, MIM# 601494 Cardiomyopathy, hypertrophic, 2, MIM# 115195