Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs112903432
rs112903432
FLNC
C 0.700 GeneticVariation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016
dbSNP: rs1446694237
rs1446694237
FLNC
T 0.700 CausalMutation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016
dbSNP: rs1554399513
rs1554399513
FLNC
CACCT 0.700 CausalMutation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016
dbSNP: rs1554400021
rs1554400021
FLNC
A 0.700 CausalMutation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016
dbSNP: rs1554401581
rs1554401581
FLNC ; FLNC-AS1
A 0.700 CausalMutation CLINVAR FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy. 28008423

2016
dbSNP: rs1554401581
rs1554401581
FLNC ; FLNC-AS1
A 0.700 CausalMutation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016
dbSNP: rs1562991776
rs1562991776
FLNC
A 0.700 GeneticVariation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016
dbSNP: rs1563005607
rs1563005607
FLNC ; FLNC-AS1
A 0.700 GeneticVariation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016
dbSNP: rs748416758
rs748416758
FLNC ; FLNC-AS1
T 0.700 CausalMutation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016
dbSNP: rs749889670
rs749889670
FLNC
G 0.700 GeneticVariation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016
dbSNP: rs774945928
rs774945928
FLNC
T 0.700 GeneticVariation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016
dbSNP: rs781135153
rs781135153
FLNC
C 0.700 CausalMutation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016
dbSNP: rs1114167361
rs1114167361
FLNC
T 0.700 CausalMutation CLINVAR Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy: Outcomes and Lessons Learned. 26436962

2015
dbSNP: rs781135153
rs781135153
FLNC
C 0.700 CausalMutation CLINVAR Prioritizing causal disease genes using unbiased genomic features. 25633252

2014
dbSNP: rs1114167361
rs1114167361
FLNC
T 0.700 CausalMutation CLINVAR LOVD v.2.0: the next generation in gene variant databases. 21520333

2011
dbSNP: rs1064795229
rs1064795229
FLNC
C 0.700 CausalMutation CLINVAR

dbSNP: rs121909518
rs121909518
FLNC ; FLNC-AS1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1402879259
rs1402879259
FLNC
TCGTCACAA 0.700 CausalMutation CLINVAR

dbSNP: rs1420159591
rs1420159591
FLNC
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554397197
rs1554397197
FLNC
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554398092
rs1554398092
FLNC
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554398674
rs1554398674
FLNC
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554400242
rs1554400242
FLNC
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554400700
rs1554400700
FLNC ; FLNC-AS1
CA 0.700 CausalMutation CLINVAR

dbSNP: rs1554401756
rs1554401756
FLNC ; FLNC-AS1
T 0.700 CausalMutation CLINVAR