{{Rsnum
|rsid=80338763
|Chromosome=17
|Orientation=minus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=PMP22
|position=15239508
|Gene_s=PMP22
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=GC
|CHROM=17
|CLNACC=RCV000020238.1; RCV000033899.2
|CLNALLE=1
|CLNDBN=Hereditary liability to pressure palsies; Charcot-Marie-Tooth disease type 2E
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1392:C0393814:162500:640:230558006; NBK1187:NBK1205:NBK1285:C1843225:607684:99939
|CLNHGVS=NC_000017.10:g.15142826dupC
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1205; NBK1392
|Disease=Hereditary liability to pressure palsies; Charcot-Marie-Tooth disease type 2E
|FwdALT=G
|GENEINFO=PMP22:5376
|GENE_ID=5376
|GENE_NAME=PMP22
|REF=G
|RSPOS=15142825
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050160000000000002110200
|WGT=0
|dbSNPBuildID=131
|rsid=80338763
}}