{{Rsnum
|rsid=71534278
|Gene=MYPN
|Chromosome=10
|position=68199417
|Orientation=plus
|GMAF=0.002296
|Gene_s=MYPN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|ALT=A,T
|CAF=0.9977; 0.002296
|CHROM=10
|CLNACC=RCV000024484.1; RCV000043541.1; RCV000043542.1
|CLNALLE=2
|CLNDBN=not provided; Dilated cardiomyopathy 1KK; Cardiomyopathy, familial hypertrophic, 22
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet; MedGen
|CLNDSDBID=CN169881:615248:154:75249; CN169882
|CLNHGVS=NC_000010.10:g.69959174C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=Leiden Muscular Dystrophy pages (MYPN); OMIM Allelic Variant
|CLNSRCID=MYPN_00003; 608517.0002
|COMMON=1
|Disease=not provided; Dilated cardiomyopathy 1KK; Cardiomyopathy
|FwdALT=A,T
|FwdREF=C
|GENEINFO=MYPN:84665
|GENE_ID=84665
|GENE_NAME=MYPN
|REF=C
|RSPOS=69959174
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000040416100100
|WGT=0
|dbSNPBuildID=130
|rsid=71534278
}}{{PMID Auto
|PMID=18006477
|Title=Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy.
}}

{{PMID Auto
|PMID=20801532
|Title=Analysis of the Z-disc genes PDLIM3 and MYPN in patients with hypertrophic cardiomyopathy.
}}

{{PMID Auto
|PMID=22286171
|Title=Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.
|OA=1
}}