Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1064795229
rs1064795229
C 0.700 CausalMutation CLINVAR

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

2011

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

2015

dbSNP: rs112903432
rs112903432
C 0.700 GeneticVariation CLINVAR Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. 27908349

2016

dbSNP: rs1402879259
rs1402879259
TCGTCACAA 0.700 CausalMutation CLINVAR

dbSNP: rs1420159591
rs1420159591
T 0.700 CausalMutation CLINVAR

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

2016

dbSNP: rs1554397197
rs1554397197
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554398092
rs1554398092
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554398674
rs1554398674
C 0.700 CausalMutation CLINVAR

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

2016

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

2016

dbSNP: rs1554400242
rs1554400242
C 0.700 CausalMutation CLINVAR

dbSNP: rs1562988883
rs1562988883
TCT 0.700 CausalMutation CLINVAR

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

2016

dbSNP: rs1562995872
rs1562995872
T 0.700 CausalMutation CLINVAR

dbSNP: rs1562998858
rs1562998858
G 0.700 CausalMutation CLINVAR

dbSNP: rs1562999451
rs1562999451
T 0.700 CausalMutation CLINVAR

dbSNP: rs1563000044
rs1563000044
T 0.700 CausalMutation CLINVAR

dbSNP: rs199976790
rs199976790
A 0.700 CausalMutation CLINVAR

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