{{Rsnum
|rsid=121913663
|Chromosome=8
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=NEFL
|position=24956098
|Gene_s=NEFL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=162280
|rsnum=121913663
|variant=0007
}}{{ClinVar
|rsid=121913663
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=24813612
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=NEFL:4747
|GENE_NAME=NEFL
|GENE_ID=4747
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.24813612C>A
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NEFL:c.418G>T; 162280.0007
|CLNSIG=5
|CLNCUI=C1843164
|CLNDBN=Charcot-Marie-Tooth disease, type IF; not provided
|Disease=Charcot-Marie-Tooth disease; not provided
|CLNACC=RCV000015079.24; RCV000057137.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1187:NBK1205:C1843164:607734:101085
}}