{{Rsnum
|rsid=119103262
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MFN2
|position=11997315
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MFN2
}}{{omim
|id=608507
|rsnum=119103262
|variant=0008
}}{{ClinVar
|rsid=119103262
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=11997315
|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.11997315C>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_014874.3:c.493C>G; 608507.0008
|CLNSIG=5
|CLNCUI=C1836485
|CLNDBN=Charcot-Marie-Tooth disease, type 2A2
|Disease=Charcot-Marie-Tooth disease
|CLNACC=RCV000002363.1
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1511:C1836485:609260:ORPHA99947
}}