{{Rsnum
|rsid=207482230
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TFG
|position=100748182
|Gene_s=TFG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=3
|CLNACC=RCV000030736.2
|CLNALLE=1
|CLNDBN=Neuropathy, hereditary motor and sensory, Okinawa type
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1858338:604484
|CLNHGVS=NC_000003.11:g.100467026C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602498.0001
|Disease=Neuropathy
|FwdALT=T
|FwdREF=C
|GENEINFO=TFG:10342
|GENE_ID=10342
|GENE_NAME=TFG
|REF=C
|RSPOS=100467026
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=207482230
}}