Incidentalome_PREGEN_DRAFT
Gene: SDHBEnsemblGeneIds (GRCh38): ENSG00000117118
EnsemblGeneIds (GRCh37): ENSG00000117118
OMIM: 185470, Gene2Phenotype
SDHB is in 13 panels
1 review
Tony Roscioli (New South Wales Health Pathology)
Comment on list classification: probably limited to adult onset disease and so should be kept on this list - needs discussionCreated: 20 Jan 2021, 5:39 a.m. | Last Modified: 20 Jan 2021, 5:39 a.m.
Panel Version: 0.40
probably limited to adult onset disease and so should be kept on this list - needs discussionCreated: 20 Jan 2021, 5:39 a.m. | Last Modified: 20 Jan 2021, 5:39 a.m.
Panel Version: 0.39
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Amber
- NSW Health Pathology
- OMIM
- 185470
- Clinvar variants
- Variants in SDHB
- Penetrance
- None
- Panels with this gene
-
- Gastrointestinal Stromal Tumour
- Paraganglioma_phaeochromocytoma
- Incidentalome
- Leukodystrophy - paediatric
- Kidney Cancer
- Additional findings_Paediatric
- Additional findings_Adult
- Incidentalome_PREGEN_DRAFT
- Pituitary Tumour
- BabyScreen+ newborn screening
- Mitochondrial disease
- Transplant Co-Morbidity Superpanel
- Cancer Predisposition_Paediatric
History Filter Activity
Entity classified by Genomics England curator
Tony Roscioli (New South Wales Health Pathology)Gene: sdhb has been classified as Amber List (Moderate Evidence).
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: SDHB was added gene: SDHB was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology Mode of inheritance for gene: SDHB was set to Unknown