{{Rsnum
|rsid=121909089
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=DNM2
|position=10793833
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DNM2
}}{{omim
|id=602378
|rsnum=121909089
|variant=0004
}}{{ClinVar
|rsid=121909089
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=10904509
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=DNM2:1785
|GENE_NAME=DNM2
|GENE_ID=1785
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.10904509G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602378.0004
|CLNSIG=5
|CLNCUI=C1834558
|CLNDBN=Myopathy, centronuclear, 1
|Disease=Myopathy
|CLNACC=RCV000007702.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1834558:160150:169189
}}