{{Rsnum
|rsid=387907035
|Chromosome=14
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=INF2
|position=104701676
|Gene_s=INF2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=14
|CLNACC=RCV000023850.1
|CLNALLE=1
|CLNDBN=Charcot-Marie-Tooth disease, dominant intermediate E
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3280845:614455:93114
|CLNHGVS=NC_000014.8:g.105168013G>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=610982.0007
|Disease=Charcot-Marie-Tooth disease
|FwdALT=T
|FwdREF=G
|REF=G
|RSPOS=105168013
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907035
|GENEINFO=INF2:64423
|GENE_ID=64423
|GENE_NAME=INF2
}}