Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1175271580
rs1175271580
LMOD2
0.010 GeneticVariation BEFREE Exome sequencing in a neonate with severe DCM revealed a homozygous nonsense variant in leiomodin 2 (<i>LMOD2</i>, p.Trp398*). 31517052

2019