Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: rs80338777
rs80338777
0.010 GeneticVariation BEFREE Cardiac dysrhythmias co-segregated with hypoKPP in one small kindred with the R528H mutation. 9132138

1997

dbSNP: rs199472936
rs199472936
0.010 GeneticVariation BEFREE Novel mechanism associated with an inherited cardiac arrhythmia: defective protein trafficking by the mutant HERG (G601S) potassium channel. 10226095

1999