KCNH2

potassium voltage-gated channel subfamily H member 2
OMIM: 152427, Gene2Phenotype

9 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 9 panels
Red KCNH2 in Hydrops fetalis Level 2: Dysmorphic and congenital abnormality syndromes Version 0.313	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Expert Review Phenotypes long QT syndrome
Green KCNH2 in Incidentalome Version 0.301	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Long QT syndrome 2, MIM# 613688 Short QT syndrome , MIM#1 609620 Tags cardiac
Green KCNH2 in Long QT Syndrome Level 2: Cardiovascular disorders Version 0.61 Component of the following Super Panels: Adult Cardiac SuperPanel Arrhythmia_SuperPanel	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes long QT syndrome
Green KCNH2 in Short QT syndrome Level 2: Cardiovascular disorders Version 1.7 Component of the following Super Panels: Adult Cardiac SuperPanel Arrhythmia_SuperPanel	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Short QT syndrome
Green KCNH2 in Additional findings_Adult Level 2: Screening Version 0.166	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance Phenotypes Long QT syndrome 2, MIM# 613688
Amber KCNH2 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber BabySeq Category B gene Phenotypes Long QT syndrome-2
Green KCNH2 in Incidentalome_PREGEN_DRAFT Version 0.43	review	Unknown	Sources NSW Health Pathology Expert Review Green
Green KCNH2 in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green BabySeq Category B gene Phenotypes Long QT syndrome 2, MIM# 613688 Tags cardiac treatable
Green KCNH2 in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Long QT syndrome 2, MIM# 613688 Short QT syndrome