SCN1B

sodium voltage-gated channel beta subunit 1
OMIM: 600235, Gene2Phenotype

9 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 9 panels
Red SCN1B in Brugada syndrome Level 2: Cardiovascular disorders Version 0.34 Component of the following Super Panels: Adult Cardiac SuperPanel Arrhythmia_SuperPanel	review	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags disputed
Green SCN1B in Incidentalome Version 0.316	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green SCN1B in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.145 Component of the following Super Panels: Progressive Neurological Conditions	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Australian Genomics Health Alliance Epilepsy Flagship Phenotypes Developmental and epileptic encephalopathy (MONDO:0100062) generalized epilepsy with febrile seizures plus (MONDO:0018214)
Green SCN1B in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.118	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genetic Health Queensland Phenotypes Epileptic encephalopathy, early infantile, 52, MIM#617350
Red SCN1B in Additional findings_Paediatric Level 2: Screening Version 0.278	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category C gene Phenotypes Brugada syndrome
Red SCN1B in Fetal anomalies Version 1.321	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red Genomics England PanelApp Genetic Health Queensland Phenotypes Epileptic encephalopathy, early infantile, 52, MIM#617350 Atrial fibrillation, familial, 13, MIM# 615377
Green SCN1B in Prepair 1000+ Level 2: Screening Version 2.7	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Developmental and epileptic encephalopathy 52, MIM#617350
Red SCN1B in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.117	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category C gene Expert Review Red Phenotypes Brugada syndrome
Amber SCN1B in Cardiac conduction disease Level 2: Cardiovascular disorders Version 1.0 Component of the following Super Panels: Adult Cardiac SuperPanel Arrhythmia_SuperPanel	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber NHS GMS Phenotypes Heart conduction disease MONDO:0000992