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 0.301	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green SCN1B in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.33 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 0.6063	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 1.255	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 Familial Generalised Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 0.14	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources GREP Expert Review Green Phenotypes Epileptic encephalopathy, early infantile, 52 617350 AR Epilepsy, generalized, with febrile seizures plus, type 1 604233 AD
No list SCN1B in Prepair 1000+ Level 2: Screening Version 1.9	review	BIALLELIC, autosomal or pseudoautosomal	Sources Literature Phenotypes Developmental and epileptic encephalopathy 52, MIM#617350
Red SCN1B in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category C gene Expert Review Red Phenotypes Brugada syndrome