Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869248137
rs869248137
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
T 0.700 CausalMutation CLINVAR

dbSNP: rs751261054
rs751261054
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
A 0.700 GeneticVariation CLINVAR

dbSNP: rs794728588
rs794728588
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
T 0.700 GeneticVariation CLINVAR

dbSNP: rs61094188
rs61094188
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
T 0.700 GeneticVariation CLINVAR

dbSNP: rs57730570
rs57730570
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
T 0.700 GeneticVariation CLINVAR

dbSNP: rs57730570
rs57730570
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
A 0.700 CausalMutation CLINVAR

dbSNP: rs397517906
rs397517906
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
T 0.700 GeneticVariation CLINVAR Heart failure in patients with arrhythmogenic right ventricular cardiomyopathy: Genetic characteristics. 30765282

2019

dbSNP: rs397517906
rs397517906
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
T 0.700 GeneticVariation CLINVAR Lamin mutation location predicts cardiac phenotype severity: combined analysis of the published literature. 30402260

2018

dbSNP: rs267607560
rs267607560
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
T 0.700 GeneticVariation CLINVAR

dbSNP: rs730880603
rs730880603
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
T 0.700 GeneticVariation CLINVAR

dbSNP: rs397516059
rs397516059
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
CA 0.700 CausalMutation CLINVAR

dbSNP: rs121909374
rs121909374
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
G 0.700 CausalMutation CLINVAR

dbSNP: rs1263987728
rs1263987728
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
C 0.700 CausalMutation CLINVAR

dbSNP: rs727504237
rs727504237
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
T 0.700 GeneticVariation CLINVAR

dbSNP: rs397516165
rs397516165
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
T 0.700 CausalMutation CLINVAR

dbSNP: rs3218716
rs3218716
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
T 0.700 CausalMutation CLINVAR

dbSNP: rs267607004
rs267607004
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
A 0.700 GeneticVariation CLINVAR

dbSNP: rs727504801
rs727504801
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
C 0.700 CausalMutation CLINVAR

dbSNP: rs1417036453
rs1417036453
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
A 0.700 CausalMutation CLINVAR

dbSNP: rs727504488
rs727504488
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
T 0.700 GeneticVariation CLINVAR

dbSNP: rs397516465
rs397516465
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
A 0.700 GeneticVariation CLINVAR

dbSNP: rs111344408
rs111344408
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
G 0.700 GeneticVariation CLINVAR

dbSNP: rs974510652
rs974510652
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
A 0.700 CausalMutation CLINVAR

dbSNP: rs878854371
rs878854371
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
G 0.700 GeneticVariation CLINVAR

dbSNP: rs869178171
rs869178171
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
A 0.700 CausalMutation CLINVAR