{{Rsnum
|rsid=121913593
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MPZ
|position=161306110
|Gene_s=MPZ
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=159440
|rsnum=121913593
|variant=0013
}}{{ClinVar
|rsid=121913593
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=161306110
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000605000002110100
|GENEINFO=MPZ:4359
|GENE_NAME=MPZ
|GENE_ID=4359
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.161306110G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000015241.21
|CLNDBN=Neuropathy, congenital hypomyelinating, autosomal dominant
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_000530.6:c.643C>T; 159440.0013
|Disease=Neuropathy
}}