{{Rsnum
|rsid=104894708
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRX
|position=40395144
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRX
}}{{omim
|id=605725
|rsnum=104894708
|variant=0008
}}{{ClinVar
|rsid=104894708
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=40901051
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=PRX:57716
|GENE_NAME=PRX
|GENE_ID=57716
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.40901051G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1468; 605725.0008
|CLNSIG=5
|CLNCUI=C0011195
|CLNDBN=Dejerine-Sottas disease; Charcot-Marie-Tooth disease, type IVF
|Disease=Dejerine-Sottas disease; Charcot-Marie-Tooth disease
|CLNACC=RCV000005061.1; RCV000032006.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1205:NBK1468:C0011195:145900:64748:111499002; NBK1358:NBK1468:CN068842:614895:99952
}}