CALM1

calmodulin 1
OMIM: 114180, ClinGen, DECIPHER

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green CALM1 in Catecholaminergic Polymorphic Ventricular Tachycardia


Level 2: Cardiovascular disorders
Version 0.37

Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Arrhythmia_SuperPanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Long QT syndrome 14 616247
    • Ventricular tachycardia, catecholaminergic polymorphic, 4 614916

    Green CALM1 in Long QT Syndrome


    Level 2: Cardiovascular disorders
    Version 0.62

    Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Arrhythmia_SuperPanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review
    Phenotypes
    • Long QT syndrome 14, MIM# 616247

    Green CALM1 in Mendeliome


    Version 1.3795

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Long QT syndrome 14 MIM#616247
    • Ventricular tachycardia, catecholaminergic polymorphic, 4 MIM#614916

    Green CALM1 in Additional findings_Adult


    Level 2: Screening
    Version 1.130

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Ventricular tachycardia, catecholaminergic polymorphic, 4 614916
    • Long QT syndrome 14, MIM# 616247

    Amber CALM1 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.141

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • ClinGen
    Phenotypes
    • Ventricular tachycardia, catecholaminergic polymorphic, 4, MIM# 614916
    Tags
    • cardiac
    • treatable

    Green CALM1 in Transplant Co-Morbidity


    Level 2: Screening
    Version 0.20

    0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Long QT syndrome 14 616247
    • Ventricular tachycardia, catecholaminergic polymorphic, 4 614916