{{Rsnum
|rsid=140148105
|Gene=MYPN
|Chromosome=10
|position=68121497
|Orientation=plus
|GMAF=0.0009183
|Gene_s=MYPN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=G
|CAF=0.9991; 0.0009183
|CHROM=10
|CLNACC=RCV000024504.1; RCV000043545.1; RCV000043546.1
|CLNALLE=1
|CLNDBN=not provided; Cardiomyopathy, familial hypertrophic, 22; Dilated cardiomyopathy 1KK
|CLNDSDB=MedGen; MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=CN169882; CN169881:615248:154:75249
|CLNHGVS=NC_000010.10:g.69881254A>G
|CLNORIGIN=33
|CLNSIG=5
|CLNSRC=Leiden Muscular Dystrophy pages (MYPN); OMIM Allelic Variant
|CLNSRCID=MYPN_00023; 608517.0004
|COMMON=0
|Disease=not provided; Cardiomyopathy; Dilated cardiomyopathy 1KK
|FwdALT=G
|FwdREF=A
|GENEINFO=MYPN:84665
|GENE_ID=84665
|GENE_NAME=MYPN
|REF=A
|RSPOS=69881254
|Reversed=0
|SAO=3
|SSR=0
|Tags=PM;PMC;SLO;VLD;KGPhase1;KGPROD;OTHERKG;LSD
|VC=SNV
|VP=0x050168000000040016100100
|WGT=0
|dbSNPBuildID=134
|rsid=140148105
}}{{PMID Auto
|PMID=22286171
|Title=Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.
|OA=1
}}