{{Rsnum
|rsid=104894075
|Chromosome=8
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=GDAP1
|position=74362940
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GDAP1
}}{{omim
|id=606598
|rsnum=104894075
|variant=0002
}}{{ClinVar
|rsid=104894075
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=75275175
|CHROM=8
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=GDAP1:54332
|GENE_NAME=GDAP1
|GENE_ID=54332
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.75275175C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606598.0002
|CLNSIG=5
|CLNCUI=C1842983; C1843183
|CLNDBN=Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4a; Charcot-Marie-Tooth disease type 2K; Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive
|Disease=Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease type 2K; Charcot-Marie-Tooth disease
|CLNACC=RCV000004410.1; RCV000004411.1; RCV000023562.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1285:NBK1468:C1842983:607831:99944; NBK1468:C1843183:607706:101097
}}