{{Rsnum
|rsid=121909091
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=DNM2
|position=10798543
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DNM2
}}{{omim
|id=602378
|rsnum=121909091
|variant=0006
}}{{ClinVar
|rsid=121909091
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=10909219
|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.10909219C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602378.0006
|CLNSIG=5
|CLNCUI=C1834558
|CLNDBN=Myopathy, centronuclear, 1
|Disease=Myopathy
|CLNACC=RCV000007704.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1834558:160150:169189
}}