{{Rsnum
|rsid=119103267
|Gene=MFN2
|Chromosome=1
|position=12009641
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MFN2
}}{{omim
|id=608507
|rsnum=119103267
|variant=0013
}}{{ClinVar
|rsid=119103267
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=12009641
|CHROM=1
|GMAF=0.0005
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000a05040016110100
|GENEINFO=MFN2:9927
|GENE_NAME=MFN2
|GENE_ID=9927
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.12009641C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_014874.3:c.2119C>T; 608507.0013
|CLNSIG=5
|CLNCUI=C1836485
|CLNDBN=Charcot-Marie-Tooth disease, type 2A2
|Disease=Charcot-Marie-Tooth disease
|CLNACC=RCV000002369.1
|Tags=PM;S3D;NSM;REF;ASP;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1511:C1836485:609260:ORPHA99947
|COMMON=0
}}