Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909091
rs121909091
DNM2
T 0.720 CausalMutation CLINVAR

dbSNP: rs121909089
rs121909089
DNM2
A 0.710 CausalMutation CLINVAR

dbSNP: rs121909090
rs121909090
DNM2
T 0.710 CausalMutation CLINVAR

dbSNP: rs587783595
rs587783595
DNM2
A 0.710 CausalMutation CLINVAR

dbSNP: rs1553742630
rs1553742630
TTN ; TTN-AS1
AC 0.700 GeneticVariation CLINVAR Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease. 25589632

2015
dbSNP: rs794729338
rs794729338
TTN ; TTN-AS1
TA 0.700 GeneticVariation CLINVAR Truncations of titin causing dilated cardiomyopathy. 22335739

2012
dbSNP: rs121909092
rs121909092
DNM2
A 0.700 CausalMutation CLINVAR

dbSNP: rs121909095
rs121909095
DNM2
T 0.700 CausalMutation CLINVAR

dbSNP: rs587783594
rs587783594
DNM2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs587783597
rs587783597
DNM2
C 0.700 CausalMutation CLINVAR

dbSNP: rs587783598
rs587783598
DNM2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs587783752
rs587783752
MTM1
CA 0.700 CausalMutation CLINVAR