{{Rsnum
|rsid=121909095
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=DNM2
|position=10823862
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DNM2
}}{{omim
|id=602378
|rsnum=121909095
|variant=0010
}}{{ClinVar
|rsid=121909095
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=10934538
|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; 2
|CLNHGVS=NC_000019.9:g.10934538C>G; NC_000019.9:g.10934538C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602378.0011; 602378.0010
|CLNSIG=5
|CLNCUI=C0410203
|CLNDBN=Severe X-linked myotubular myopathy
|Disease=Severe X-linked myotubular myopathy
|CLNACC=RCV000007709.1; RCV000007708.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1432:C0410203:310400:596:46804001
}}