Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1564526327
rs1564526327
A 0.700 GeneticVariation CLINVAR

dbSNP: rs774870551
rs774870551
VCL
0.010 GeneticVariation BEFREE We have identified the cardiomyopathy-susceptibility gene vinculin (<i>VCL</i>) mutation M94I may account for a sudden unexplained nocturnal death syndrome (SUNDS) case. 28373245

2017

dbSNP: rs4746172
rs4746172
VCL
0.010 GeneticVariation BEFREE The VCL-encoding protein was involved in cardiomyopathy that associated with hypertension, therefore our results suggest the rs4746172 of VCL may be a novel target for clinical interventions to reduce CVD risk by regulating blood pressure in male Chinese. 26487440

2015

dbSNP: rs121917776
rs121917776
VCL
0.010 GeneticVariation BEFREE Finally, the cardiomyopathy associated DeltaLeu954 and Arg975Trp metavinculin mutants reside on the replaced extended coil and the H1' alpha-helix, respectively. 20502710

2010