SDHAF2

succinate dehydrogenase complex assembly factor 2
OMIM: 613019, Gene2Phenotype

11 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 11 panels
Green SDHAF2 in Incidentalome Version 0.301	review	Unknown	Sources Expert Review Green Melbourne Genomics Health Alliance Victorian Clinical Genetics Services Expert Review Green
Green SDHAF2 in Cancer Predisposition_Paediatric Level 2: Cancer Version 0.131	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Paragangliomas 2, MIM# 601650
Red SDHAF2 in Mitochondrial disease Level 2: Metabolic disorders Version 0.927 Component of the following Super Panels: Metabolic Disorders Superpanel Progressive Neurological Conditions	review	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Australian Genomics Health Alliance Mitochondrial Flagship Phenotypes Paragangliomas 2, MIM# 601650
Green SDHAF2 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 Paragangliomas 2, MIM# 601650
Red SDHAF2 in CGC_86 Version 0.2	review	Other	Sources CGC_86 Phenotypes Hereditary Paraganglioma-Pheochromocytoma Syndromes
Red SDHAF2 in NCGC Version 0.2	review	Other	Sources NCGC Phenotypes Hereditary Paraganglioma-Pheochromocytoma Syndromes
Red SDHAF2 in TCGA_PANCAN_2018 Version 0.2	review	Other	Sources TCGA_PANCAN_2018 Phenotypes Hereditary Paraganglioma-Pheochromocytoma Syndromes
Amber SDHAF2 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 Hereditary Paraganglioma-Pheochromocytoma Syndromes
Amber SDHAF2 in Incidentalome_PREGEN_DRAFT Version 0.43	review	Unknown	Sources Expert Review Amber NSW Health Pathology
Amber SDHAF2 in BabyScreen+ newborn screening Level 2: Screening Version 1.114	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category B gene Expert Review Amber Phenotypes Hereditary Paraganglioma-Pheochromocytoma Syndromes
Green SDHAF2 in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance Phenotypes Paragangliomas 2, MIM# 601650