{{Rsnum
|rsid=121913589
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MPZ
|position=161306863
|Gene_s=MPZ
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=159440
|rsnum=121913589
|variant=0009
}}{{ClinVar
|rsid=121913589
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=161306863
|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; 2
|CLNHGVS=NC_000001.11:g.161306863C>G; NC_000001.11:g.161306863C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000530.6:c.293G>C; 159440.0009; NM_000530.6:c.293G>A; 159440.0011
|CLNSIG=5
|CLNCUI=C0270912
|CLNDBN=Charcot-Marie-Tooth disease, type IB
|Disease=Charcot-Marie-Tooth disease
|CLNACC=RCV000015237.24; RCV000015239.20
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1205:C0270912:118200:ORPHA101082:42986003
}}