Incidentalome_PREGEN_DRAFT

Gene: SDHD

Red List (low evidence)

SDHD (succinate dehydrogenase complex subunit D)
EnsemblGeneIds (GRCh38): ENSG00000204370
EnsemblGeneIds (GRCh37): ENSG00000204370
OMIM: 602690, Gene2Phenotype
SDHD is in 13 panels

1 review

Tony Roscioli (New South Wales Health Pathology)

Red List (low evidence)

Comment on list classification: may cause childhood onset disease
Created: 20 Jan 2021, 5:37 a.m. | Last Modified: 20 Jan 2021, 5:37 a.m.
Panel Version: 0.39
may cause childhood onset disease
Created: 20 Jan 2021, 5:37 a.m. | Last Modified: 20 Jan 2021, 5:37 a.m.
Panel Version: 0.38

History Filter Activity

20 Jan 2021, Gel status: 1

Entity classified by Genomics England curator

Tony Roscioli (New South Wales Health Pathology)

Gene: sdhd has been classified as Red List (Low Evidence).

9 Nov 2020, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: SDHD was added gene: SDHD was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology Mode of inheritance for gene: SDHD was set to Unknown