Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398124650
rs398124650
CALM2
T 0.800 GeneticVariation CLINVAR

dbSNP: rs398124650
rs398124650
CALM2
G 0.800 CausalMutation CLINVAR

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

2013
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 Distinctive malfunctions of calmodulin mutations associated with heart RyR2-mediated arrhythmic disease. 26164367

2015
dbSNP: rs398124650
rs398124650
CALM2
0.800 GeneticVariation UNIPROT Arrhythmogenic calmodulin mutations impede activation of small-conductance calcium-activated potassium current. 27165696

2016
dbSNP: rs730882252
rs730882252
CALM1
0.700 GeneticVariation UNIPROT

dbSNP: rs730882254
rs730882254
CALM2
A 0.700 CausalMutation CLINVAR