{{Rsnum
|rsid=104894077
|Gene=GDAP1
|Chromosome=8
|position=74361886
|Orientation=plus
|GMAF=0.0
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=GDAP1
}}{{omim
|id=606598
|rsnum=104894077
|variant=0004
}}{{ClinVar
|rsid=104894077
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=75274121
|CHROM=8
|GMAF=0
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000016110100
|GENEINFO=GDAP1:54332
|GENE_NAME=GDAP1
|GENE_ID=54332
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.75274121C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;SLO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=1; 0
|CLNACC=RCV000004413.1; RCV000031963.1
|CLNDBN=Neuropathy, axonal, with vocal cord paresis, autosomal recessive; Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1468:C1843183:607706:101097
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1468; 606598.0004
|COMMON=0
|Disease=Neuropathy; Charcot-Marie-Tooth disease
}}