Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397517906
rs397517906
T 0.700 GeneticVariation CLINVAR Heart failure in patients with arrhythmogenic right ventricular cardiomyopathy: Genetic characteristics. 30765282

2019

dbSNP: rs397517906
rs397517906
T 0.700 GeneticVariation CLINVAR Lamin mutation location predicts cardiac phenotype severity: combined analysis of the published literature. 30402260

2018

dbSNP: rs111344408
rs111344408
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1131691655
rs1131691655
C 0.700 CausalMutation CLINVAR

dbSNP: rs121909374
rs121909374
G 0.700 CausalMutation CLINVAR

dbSNP: rs1263987728
rs1263987728
C 0.700 CausalMutation CLINVAR

dbSNP: rs1417036453
rs1417036453
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553692290
rs1553692290
T 0.700 CausalMutation CLINVAR

dbSNP: rs267607004
rs267607004
A 0.700 GeneticVariation CLINVAR

dbSNP: rs267607560
rs267607560
T 0.700 GeneticVariation CLINVAR

dbSNP: rs3218716
rs3218716
T 0.700 CausalMutation CLINVAR

dbSNP: rs371678190
rs371678190
A 0.700 CausalMutation CLINVAR

dbSNP: rs397516059
rs397516059
CA 0.700 CausalMutation CLINVAR

dbSNP: rs397516165
rs397516165
T 0.700 CausalMutation CLINVAR

dbSNP: rs397516465
rs397516465
A 0.700 GeneticVariation CLINVAR

dbSNP: rs397517689
rs397517689
A 0.700 CausalMutation CLINVAR

dbSNP: rs57730570
rs57730570
T 0.700 GeneticVariation CLINVAR

dbSNP: rs57730570
rs57730570
A 0.700 CausalMutation CLINVAR

dbSNP: rs61094188
rs61094188
T 0.700 GeneticVariation CLINVAR

dbSNP: rs72648250
rs72648250
A 0.700 CausalMutation CLINVAR

dbSNP: rs727503533
rs727503533
T 0.700 GeneticVariation CLINVAR

dbSNP: rs727503607
rs727503607
A 0.700 CausalMutation CLINVAR

dbSNP: rs727504237
rs727504237
T 0.700 GeneticVariation CLINVAR

dbSNP: rs727504488
rs727504488
T 0.700 GeneticVariation CLINVAR

dbSNP: rs727504801
rs727504801
C 0.700 CausalMutation CLINVAR