Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912775
rs121912775
CACNA1C
A 0.700 CausalMutation CLINVAR Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death. 17224476

2007
dbSNP: rs121912776
rs121912776
CACNA1C
T 0.700 CausalMutation CLINVAR Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death. 17224476

2007