{{Rsnum
|rsid=119103266
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MFN2
|position=11998787
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MFN2
}}{{omim
|id=608507
|rsnum=119103266
|variant=0012
}}{{ClinVar
|rsid=119103266
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=11998787
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=MFN2:9927
|GENE_NAME=MFN2
|GENE_ID=9927
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.11998787C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_014874.3:c.617C>T; 608507.0012
|CLNSIG=5
|CLNCUI=C0393807
|CLNDBN=Hereditary motor and sensory neuropathy with optic atrophy
|Disease=Hereditary motor and sensory neuropathy with optic atrophy
|CLNACC=RCV000002368.1
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0393807:601152:128203003
}}