{{Rsnum
|rsid=199476408
|Chromosome=10
|position=68165803
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYPN
|Gene_s=MYPN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=T
|CHROM=10
|CLNACC=RCV000024509.1; RCV000043547.1
|CLNALLE=1
|CLNDBN=not provided; Cardiomyopathy, familial restrictive, 4
|CLNDSDB=MedGen
|CLNDSDBID=CN169883
|CLNHGVS=NC_000010.10:g.69925560C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=Leiden Muscular Dystrophy pages (MYPN); OMIM Allelic Variant
|CLNSRCID=MYPN_00028; 608517.0005
|Disease=not provided; Cardiomyopathy
|FwdALT=T
|FwdREF=C
|GENEINFO=MYPN:84665
|GENE_ID=84665
|GENE_NAME=MYPN
|REF=C
|RSPOS=69925560
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=199476408
}}{{PMID Auto
|PMID=22286171
|Title=Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.
|OA=1
}}