{{Rsnum
|rsid=387907036
|Chromosome=14
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=INF2
|position=104701677
|Gene_s=INF2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=14
|CLNACC=RCV000023851.1
|CLNALLE=1
|CLNDBN=Charcot-Marie-Tooth disease, dominant intermediate E
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3280845:614455:93114
|CLNHGVS=NC_000014.8:g.105168014C>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=610982.0008
|Disease=Charcot-Marie-Tooth disease
|FwdALT=G
|FwdREF=C
|REF=C
|RSPOS=105168014
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907036
|GENEINFO=INF2:64423
|GENE_ID=64423
|GENE_NAME=INF2
}}