Incidentalome_PREGEN_DRAFT
Gene: SDHAF2EnsemblGeneIds (GRCh38): ENSG00000167985
EnsemblGeneIds (GRCh37): ENSG00000167985
OMIM: 613019, Gene2Phenotype
SDHAF2 is in 11 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, 5:40 a.m. | Last Modified: 20 Jan 2021, 5:40 a.m.
Panel Version: 0.41
probably limited to adult onset disease and so should be kept on this list - needs discussionCreated: 20 Jan 2021, 5:40 a.m. | Last Modified: 20 Jan 2021, 5:40 a.m.
Panel Version: 0.40
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Amber
- NSW Health Pathology
- OMIM
- 613019
- Clinvar variants
- Variants in SDHAF2
- Penetrance
- None
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Tony Roscioli (New South Wales Health Pathology)Gene: sdhaf2 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: SDHAF2 was added gene: SDHAF2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology Mode of inheritance for gene: SDHAF2 was set to Unknown