{{Rsnum
|rsid=121913605
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MPZ
|position=161307306
|Gene_s=MPZ
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=159440
|rsnum=121913605
|variant=0029
}}{{ClinVar
|rsid=121913605
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=161307306
|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.161307306G>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000530.6:c.186C>G; 159440.0029
|CLNSIG=5
|CLNCUI=C1843251
|CLNDBN=Charcot-Marie-Tooth disease type 2I
|Disease=Charcot-Marie-Tooth disease type 2I
|CLNACC=RCV000015258.24
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1205:NBK1285:C1843251:607677:ORPHA99942
}}