{{Rsnum
|rsid=121909088
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=DNM2
|position=10819992
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DNM2
}}{{omim
|id=602378
|rsnum=121909088
|variant=0002
}}{{ClinVar
|rsid=121909088
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=10930668
|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.10930668A>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000007700.1
|CLNDBN=Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia
|CLNDSDB=MedGen
|CLNDSDBID=C2751367
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602378.0002
|Disease=Charcot-Marie-Tooth disease
}}