{{Rsnum
|rsid=121908531
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=DNM1L
|position=32731118
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DNM1L,YARS2
}}{{omim
|id=603850
|rsnum=121908531
|variant=0001
}}{{ClinVar
|rsid=121908531
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=32884052
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=DNM1L:10059
|GENE_NAME=DNM1L
|GENE_ID=10059
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.32884052C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603850.0001
|CLNSIG=5
|CLNCUI=CN119491
|CLNDBN=Encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission
|Disease=Encephalopathy
|CLNACC=RCV000006386.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3280660:614388:330050
}}