{{Rsnum
|rsid=119103265
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MFN2
|position=12002033
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MFN2
}}{{omim
|id=608507
|rsnum=119103265
|variant=0011
}}{{ClinVar
|rsid=119103265
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=12002033
|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.12002033C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_014874.3:c.1090C>T; 608507.0011
|CLNSIG=5
|CLNCUI=C0393807; C1836485
|CLNDBN=Hereditary motor and sensory neuropathy with optic atrophy; Charcot-Marie-Tooth disease, type 2A2
|Disease=Hereditary motor and sensory neuropathy with optic atrophy; Charcot-Marie-Tooth disease
|CLNACC=RCV000002367.1; RCV000023711.1
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C0393807:601152:128203003; NBK1511:C1836485:609260:ORPHA99947
}}