Gene: CALM1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607277
rs267607277
CALM1
0.710 GeneticVariation BEFREE A second, de novo, missense mutation (c.293A>G [p.Asn97Ser]) was subsequently identified in an individual of Iraqi origin; this individual was diagnosed with CPVT from a screening of 61 arrhythmia samples with no identified RYR2 mutations. 23040497

2012
dbSNP: rs267607277
rs267607277
CALM1
G 0.710 GeneticVariation CLINVAR

dbSNP: rs267607276
rs267607276
CALM1
T 0.700 GeneticVariation CLINVAR