{{Rsnum
|rsid=121913595
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MPZ
|position=161306785
|Gene_s=MPZ
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=159440
|rsnum=121913595
|variant=0016
}}{{ClinVar
|rsid=121913595
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=161306785
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000a05000002110100
|GENEINFO=MPZ:4359
|GENE_NAME=MPZ
|GENE_ID=4359
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000001.11:g.161306785G>A; NC_000001.11:g.161306785G>T
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000530.6:c.371C>T; NBK1205; 159440.0016; NM_000530.6:c.371C>A; 159440.0031
|CLNSIG=5
|CLNCUI=C1843153; C0270912
|CLNDBN=Charcot-Marie-Tooth disease type 2J; Charcot-Marie-Tooth disease, type IB; Neuropathy, congenital hypomyelinating, autosomal dominant
|Disease=Charcot-Marie-Tooth disease type 2J; Charcot-Marie-Tooth disease; Neuropathy
|CLNACC=RCV000015244.24; RCV000015245.21; RCV000015260.20
|Tags=RV;PM;S3D;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1205:NBK1285:C1843153:607736:ORPHA99943; NBK1205:C0270912:118200:ORPHA101082:42986003
}}