{{Rsnum
|rsid=104894623
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=PMP22
|position=15239591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PMP22
}}{{omim
|id=601097
|rsnum=104894623
|variant=0010
}}
{{omim
|id=601097
|rsnum=104894623
|variant=0017
}}{{ClinVar
|rsid=104894623
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=15142908
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=PMP22:5376
|GENE_NAME=PMP22
|GENE_ID=5376
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000017.10:g.15142908C>G; NC_000017.10:g.15142908C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1205; 601097.0010; 601097.0017
|CLNSIG=5
|CLNCUI=C1861669; C0393814
|CLNDBN=Charcot-Marie-Tooth disease, type IE; Hereditary liability to pressure palsies
|Disease=Charcot-Marie-Tooth disease; Hereditary liability to pressure palsies
|CLNACC=RCV000008951.1; RCV000008956.2
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1205:C1861669:118300:90658; NBK1392:C0393814:162500:640:230558006
}}