{{Rsnum
|rsid=121913601
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MPZ
|position=161307259
|Gene_s=MPZ
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=159440
|rsnum=121913601
|variant=0023
}}{{ClinVar
|rsid=121913601
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=161307259
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=MPZ:4359
|GENE_NAME=MPZ
|GENE_ID=4359
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.161307259G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000015252.20
|CLNDBN=Charcot-Marie-Tooth disease, type 1b, with focally folded myelin sheaths
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_000530.6:c.233C>T; 159440.0023
|Disease=Charcot-Marie-Tooth disease
}}