{{Rsnum
|rsid = 28940293
|Gene = MFN2
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|Chromosome=1
|position=11992606
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MFN2
}}{{omim
|desc=CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2
|id=608507
|rsnum=28940293
|variant=0003
}}
{{ neighbor
| rsid = 28940296
| distance = 22
}}
{{ neighbor
| rsid = 28940291
| distance = 54
}}{{ClinVar
|rsid=28940293
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=11992606
|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.11992606T>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_014874.3:c.227T>C; 608507.0003
|CLNSIG=5
|CLNCUI=C1836485
|CLNDBN=Charcot-Marie-Tooth disease, type 2A2
|Disease=Charcot-Marie-Tooth disease
|CLNACC=RCV000002358.1
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1511:C1836485:609260:ORPHA99947
}}