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Brugada syndrome (Version 0.34)

Level 2: Cardiovascular disorders

Panel types: Victorian Clinical Genetics Services, Rare Disease
Description
This panel was developed and is maintained by VCGS.
Panel Activity

4 reviewers

  • Ivan Macciocca (Victorian Clinical Genetics Services)

  • Elena Savva (Victorian Clinical Genetics Services)

  • Bryony Thompson (Royal Melbourne Hospital)

  • Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

11 Entities

11 reviewed, 1 green

List Entity Reviews Mode of inheritance Details
11 Entitiess
Green List (high evidence)
SCN5A
2 reviews
2 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Atrial fibrillation, familial, 10
  • Brugada syndrome 1
  • Cardiomyopathy, dilated, 1E
  • Heart block, nonprogressive
  • Heart block, progressive, type IA
  • Long QT syndrome 3
  • Sick sinus syndrome 1
  • Ventricular fibrillation, familial, 1
  • {Sudden infant death syndrome, susceptibility to}
Tags
Red List (low evidence)
CACNA1C
1 review
1 red 		Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Tags
  • disputed
Red List (low evidence)
CACNA2D1
1 review
1 red 		Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Tags
  • disputed
Red List (low evidence)
CACNB2
1 review
1 red 		Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Tags
  • disputed
Red List (low evidence)
GPD1L
3 reviews
1 red 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Brugada syndrome 2, MIM# 611777
Tags
  • disputed
Red List (low evidence)
KCND3
1 review
1 red 		Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Brugada syndrome
Tags
  • disputed
Red List (low evidence)
KCNE3
1 review
1 red 		Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Tags
  • disputed
Red List (low evidence)
KCNJ8
1 review
1 red 		Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Brugada syndrome
Tags
  • disputed
Red List (low evidence)
SCN10A
1 review
1 red 		Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Brugada syndrome
Tags
  • disputed
Red List (low evidence)
SCN1B
1 review
1 red 		Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Tags
  • disputed
Red List (low evidence)
SCN3B
2 reviews
2 red 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Brugada syndrome 7 MIM#613120
Tags
  • disputed

Downloads

Download lists

  • Whole panel
  • Green list (high evidence)
  • Green and Amber Genes
  • Amber Genes
  • Red list (low evidence)

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