{{Rsnum
|rsid=121913586
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MPZ
|position=161306414
|Gene_s=MPZ
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=159440
|rsnum=121913586
|variant=0005
}}{{ClinVar
|rsid=121913586
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=161306414
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000a05000002110100
|GENEINFO=MPZ:4359
|GENE_NAME=MPZ
|GENE_ID=4359
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.161306414C>G
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000530.6:c.499G>C; NBK1205; 159440.0005
|CLNSIG=5
|CLNCUI=CN069174
|CLNDBN=Dejerine-Sottas syndrome, autosomal dominant; Dejerine-Sottas disease
|Disease=Dejerine-Sottas syndrome; Dejerine-Sottas disease
|CLNACC=RCV000015233.24; RCV000032123.1
|Tags=RV;PM;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=CN069174; NBK1205:C0011195:145900:ORPHA64748:111499002
}}