Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398124647
rs398124647
CALM2
0.800 GeneticVariation UNIPROT Arrhythmogenic calmodulin mutations impede activation of small-conductance calcium-activated potassium current. 27165696

2016
dbSNP: rs398124647
rs398124647
CALM2
0.800 GeneticVariation UNIPROT Novel CPVT-Associated Calmodulin Mutation in CALM3 (CALM3-A103V) Activates Arrhythmogenic Ca Waves and Sparks. 27516456

2016
dbSNP: rs398124647
rs398124647
CALM2
0.800 GeneticVariation UNIPROT Spectrum and Prevalence of CALM1-, CALM2-, and CALM3-Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome-Associated Calmodulin Missense Variant, E141G. 26969752

2016
dbSNP: rs398124648
rs398124648
CALM2
0.800 GeneticVariation UNIPROT Novel CPVT-Associated Calmodulin Mutation in CALM3 (CALM3-A103V) Activates Arrhythmogenic Ca Waves and Sparks. 27516456

2016
dbSNP: rs398124648
rs398124648
CALM2
0.800 GeneticVariation UNIPROT Arrhythmogenic calmodulin mutations impede activation of small-conductance calcium-activated potassium current. 27165696

2016
dbSNP: rs398124648
rs398124648
CALM2
0.800 GeneticVariation UNIPROT Spectrum and Prevalence of CALM1-, CALM2-, and CALM3-Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome-Associated Calmodulin Missense Variant, E141G. 26969752

2016
dbSNP: rs398124649
rs398124649
CALM2
0.800 GeneticVariation UNIPROT Arrhythmogenic calmodulin mutations impede activation of small-conductance calcium-activated potassium current. 27165696

2016
dbSNP: rs398124649
rs398124649
CALM2
0.800 GeneticVariation UNIPROT Spectrum and Prevalence of CALM1-, CALM2-, and CALM3-Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome-Associated Calmodulin Missense Variant, E141G. 26969752

2016
dbSNP: rs398124649
rs398124649
CALM2
0.800 GeneticVariation UNIPROT Novel CPVT-Associated Calmodulin Mutation in CALM3 (CALM3-A103V) Activates Arrhythmogenic Ca Waves and Sparks. 27516456

2016
dbSNP: rs398124650
rs398124650
CALM2
0.800 GeneticVariation UNIPROT Spectrum and Prevalence of CALM1-, CALM2-, and CALM3-Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome-Associated Calmodulin Missense Variant, E141G. 26969752

2016
dbSNP: rs398124650
rs398124650
CALM2
0.800 GeneticVariation UNIPROT Novel CPVT-Associated Calmodulin Mutation in CALM3 (CALM3-A103V) Activates Arrhythmogenic Ca Waves and Sparks. 27516456

2016
dbSNP: rs398124650
rs398124650
CALM2
0.800 GeneticVariation UNIPROT Arrhythmogenic calmodulin mutations impede activation of small-conductance calcium-activated potassium current. 27165696

2016
dbSNP: rs398124647
rs398124647
CALM2
0.800 GeneticVariation UNIPROT Distinctive malfunctions of calmodulin mutations associated with heart RyR2-mediated arrhythmic disease. 26164367

2015
dbSNP: rs398124648
rs398124648
CALM2
0.800 GeneticVariation UNIPROT Distinctive malfunctions of calmodulin mutations associated with heart RyR2-mediated arrhythmic disease. 26164367

2015
dbSNP: rs398124649
rs398124649
CALM2
0.800 GeneticVariation UNIPROT Distinctive malfunctions of calmodulin mutations associated with heart RyR2-mediated arrhythmic disease. 26164367

2015
dbSNP: rs398124650
rs398124650
CALM2
0.800 GeneticVariation UNIPROT Distinctive malfunctions of calmodulin mutations associated with heart RyR2-mediated arrhythmic disease. 26164367

2015
dbSNP: rs398124647
rs398124647
CALM2
0.800 GeneticVariation UNIPROT Novel calmodulin mutations associated with congenital arrhythmia susceptibility. 24917665

2014
dbSNP: rs398124648
rs398124648
CALM2
0.800 GeneticVariation UNIPROT Novel calmodulin mutations associated with congenital arrhythmia susceptibility. 24917665

2014
dbSNP: rs398124649
rs398124649
CALM2
0.800 GeneticVariation UNIPROT Novel calmodulin mutations associated with congenital arrhythmia susceptibility. 24917665

2014
dbSNP: rs398124650
rs398124650
CALM2
0.800 GeneticVariation UNIPROT Novel calmodulin mutations associated with congenital arrhythmia susceptibility. 24917665

2014
dbSNP: rs398124647
rs398124647
CALM2
0.800 GeneticVariation UNIPROT Calmodulin mutations associated with recurrent cardiac arrest in infants. 23388215

2013
dbSNP: rs398124648
rs398124648
CALM2
0.800 GeneticVariation UNIPROT Calmodulin mutations associated with recurrent cardiac arrest in infants. 23388215

2013
dbSNP: rs398124649
rs398124649
CALM2
0.800 GeneticVariation UNIPROT Calmodulin mutations associated with recurrent cardiac arrest in infants. 23388215

2013
dbSNP: rs398124650
rs398124650
CALM2
0.800 GeneticVariation UNIPROT Calmodulin mutations associated with recurrent cardiac arrest in infants. 23388215

2013
dbSNP: rs398124647
rs398124647
CALM2
A 0.800 CausalMutation CLINVAR