Gene: RBM20 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs794729157
rs794729157
RBM20
0.010 GeneticVariation BEFREE In the present study, we identified an R634W missense mutation within the stretch and a G1031X nonsense mutation in cohorts of DCM patients. 29895960

2018
dbSNP: rs397516607
rs397516607
RBM20
0.010 GeneticVariation BEFREE We identified a family with DCM carrying a mutation (RBM20(E913K/+)) in a glutamate-rich region of RBM20. 27496873

2016