Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28933093
rs28933093
A 0.810 CausalMutation CLINVAR

dbSNP: rs56984562
rs56984562
G 0.810 CausalMutation CLINVAR

dbSNP: rs267607570
rs267607570
C 0.800 GeneticVariation CLINVAR

dbSNP: rs28928900
rs28928900
G 0.800 CausalMutation CLINVAR

dbSNP: rs28933090
rs28933090
G 0.800 CausalMutation CLINVAR

dbSNP: rs28933091
rs28933091
G 0.800 CausalMutation CLINVAR

dbSNP: rs28933092
rs28933092
G 0.800 CausalMutation CLINVAR

dbSNP: rs60890628
rs60890628
T 0.800 CausalMutation CLINVAR

dbSNP: rs11575937
rs11575937
A 0.700 CausalMutation CLINVAR

dbSNP: rs1165819867
rs1165819867
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1553265180
rs1553265180
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1553265736
rs1553265736
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1553265739
rs1553265739
T 0.700 GeneticVariation CLINVAR

dbSNP: rs267607581
rs267607581
G 0.700 CausalMutation CLINVAR

dbSNP: rs386134243
rs386134243
T 0.700 CausalMutation CLINVAR

dbSNP: rs397517889
rs397517889
T 0.700 GeneticVariation CLINVAR

dbSNP: rs397517889
rs397517889
T 0.700 CausalMutation CLINVAR

dbSNP: rs56771886
rs56771886
C 0.700 CausalMutation CLINVAR

dbSNP: rs57077886
rs57077886
T 0.700 CausalMutation CLINVAR

dbSNP: rs58362413
rs58362413
A 0.700 CausalMutation CLINVAR

dbSNP: rs59332535
rs59332535
A 0.700 CausalMutation CLINVAR

dbSNP: rs59684335
rs59684335
C 0.700 CausalMutation CLINVAR

dbSNP: rs730882262
rs730882262
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057515421
rs1057515421
T 0.700 CausalMutation CLINVAR Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. 10580070

1999

dbSNP: rs56984562
rs56984562
T 0.810 CausalMutation CLINVAR Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation. 14675861

2003