Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1562999451
rs1562999451
T 0.700 CausalMutation CLINVAR

dbSNP: rs1563000044
rs1563000044
T 0.700 CausalMutation CLINVAR

dbSNP: rs1563001456
rs1563001456
T 0.700 CausalMutation CLINVAR

dbSNP: rs1563001548
rs1563001548
A 0.700 CausalMutation CLINVAR

dbSNP: rs1563003153
rs1563003153
A 0.700 CausalMutation CLINVAR

dbSNP: rs1563005607
rs1563005607
A 0.700 GeneticVariation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016

dbSNP: rs199976790
rs199976790
A 0.700 CausalMutation CLINVAR

dbSNP: rs748416758
rs748416758
T 0.700 CausalMutation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016

dbSNP: rs749889670
rs749889670
G 0.700 GeneticVariation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016

dbSNP: rs755583250
rs755583250
T 0.700 CausalMutation CLINVAR

dbSNP: rs763330423
rs763330423
C 0.700 GeneticVariation CLINVAR

dbSNP: rs766330686
rs766330686
T 0.700 CausalMutation CLINVAR

dbSNP: rs770606675
rs770606675
T 0.700 CausalMutation CLINVAR

dbSNP: rs774945928
rs774945928
T 0.700 GeneticVariation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016

dbSNP: rs781135153
rs781135153
C 0.700 CausalMutation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016

dbSNP: rs781135153
rs781135153
C 0.700 CausalMutation CLINVAR Prioritizing causal disease genes using unbiased genomic features. 25633252

2014