{{Rsnum
|rsid=199422214
|Chromosome=8
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=NEFL
|position=24955888
|Gene_s=NEFL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=8
|CLNACC=RCV000022674.24
|CLNALLE=1
|CLNDBN=Charcot-Marie-Tooth disease, type IF
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1187:NBK1205:C1843164:607734:101085
|CLNHGVS=NC_000008.10:g.24813402C>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=162280.0008
|Disease=Charcot-Marie-Tooth disease
|FwdALT=T
|FwdREF=G
|GENEINFO=NEFL:4747
|GENE_ID=4747
|GENE_NAME=NEFL
|REF=C
|RSPOS=24813402
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD
|VC=SNV
|VP=0x050068000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=199422214
}}{{PMID Auto
|PMID=20039262
|Title=A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy.
}}