Incidentalome_PREGEN_DRAFT
Gene: SRD5A2EnsemblGeneIds (GRCh38): ENSG00000277893
EnsemblGeneIds (GRCh37): ENSG00000049319
OMIM: 607306, Gene2Phenotype
SRD5A2 is in 4 panels
1 review
Tony Roscioli (New South Wales Health Pathology)
Comment on list classification: Needs discussion due to clinical featuresCreated: 20 Jan 2021, 5:29 a.m. | Last Modified: 20 Jan 2021, 5:29 a.m.
Panel Version: 0.35
Needs discussion due to clinical featuresCreated: 20 Jan 2021, 5:28 a.m. | Last Modified: 20 Jan 2021, 5:28 a.m.
Panel Version: 0.34
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Amber
- NSW Health Pathology
- OMIM
- 607306
- Clinvar variants
- Variants in SRD5A2
- Penetrance
- None
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Tony Roscioli (New South Wales Health Pathology)Gene: srd5a2 has been classified as Amber List (Moderate Evidence).
Entity classified by Genomics England curator
Tony Roscioli (New South Wales Health Pathology)Gene: srd5a2 has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: SRD5A2 was added gene: SRD5A2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology Mode of inheritance for gene: SRD5A2 was set to Unknown