Cardiac arrhythmias - previous panel
Gene: SCN10AEnsemblGeneIds (GRCh38): ENSG00000185313
EnsemblGeneIds (GRCh37): ENSG00000185313
OMIM: 604427, Gene2Phenotype
SCN10A is in 7 panels
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Green
- Phenotypes
-
- J wave syndrome
- sudden death
- short QT
- OMIM
- 604427
- Clinvar variants
- Variants in SCN10A
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Panel promoted to version 1.0
Ellen McDonagh (Genomics England Curator)Checked against the component panels, and ready to be promoted to version 1.
Set Phenotypes
Rebecca Foulger (Genomics England curator)Added phenotypes J wave syndrome; sudden death; short QT for gene: SCN10A
Created, Added New Source, Set mode of inheritance, Set publications
Rebecca Foulger (Genomics England curator)gene: SCN10A was added gene: SCN10A was added to Cardiac arrythmias. Sources: Expert Review Green Mode of inheritance for gene: SCN10A was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: SCN10A were set to 29016797; 24998131; 30177317