Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs879253730
rs879253730
C 0.700 CausalMutation CLINVAR Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young. 27435932

2016

dbSNP: rs397508087
rs397508087
A 0.700 CausalMutation CLINVAR

dbSNP: rs397508101
rs397508101
T 0.700 CausalMutation CLINVAR

dbSNP: rs74315447
rs74315447
C 0.700 GeneticVariation CLINVAR

dbSNP: rs794728425
rs794728425
CGGGGCGATGGGAGCTGGCCG 0.700 CausalMutation CLINVAR

dbSNP: rs794728426
rs794728426
GCTTTT 0.700 CausalMutation CLINVAR

dbSNP: rs794728428
rs794728428
T 0.700 CausalMutation CLINVAR

dbSNP: rs794728434
rs794728434
TGCAG 0.700 CausalMutation CLINVAR

dbSNP: rs794728456
rs794728456
C 0.700 CausalMutation CLINVAR

dbSNP: rs794728457
rs794728457
G 0.700 CausalMutation CLINVAR

dbSNP: rs794728464
rs794728464
CGCCT 0.700 CausalMutation CLINVAR

dbSNP: rs794728465
rs794728465
AG 0.700 CausalMutation CLINVAR

dbSNP: rs794728467
rs794728467
GCCGC 0.700 CausalMutation CLINVAR

dbSNP: rs794728470
rs794728470
ACGTCGCCC 0.700 CausalMutation CLINVAR

dbSNP: rs794728472
rs794728472
T 0.700 CausalMutation CLINVAR

dbSNP: rs794728476
rs794728476
CCTGCGCGAT 0.700 CausalMutation CLINVAR

dbSNP: rs794728489
rs794728489
ACCAC 0.700 CausalMutation CLINVAR

dbSNP: rs794728497
rs794728497
G 0.700 CausalMutation CLINVAR

dbSNP: rs794728499
rs794728499
A 0.700 CausalMutation CLINVAR

dbSNP: rs794728500
rs794728500
C 0.700 CausalMutation CLINVAR

dbSNP: rs794728506
rs794728506
G 0.700 CausalMutation CLINVAR

dbSNP: rs794728507
rs794728507
A 0.700 CausalMutation CLINVAR

dbSNP: rs794728508
rs794728508
C 0.700 CausalMutation CLINVAR

dbSNP: rs794728563
rs794728563
T 0.700 CausalMutation CLINVAR

dbSNP: rs3745297
rs3745297
HRC
0.040 GeneticVariation BEFREE Herein, we summarize the current evidence on the pivotal role of HRC in the regulation of cardiac rhythmicity and the importance of HRC Ser96Ala as a genetic modifier for arrhythmias in the setting of heart failure. 30319456

2018