{{Rsnum
|rsid=104894706
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRX
|position=40397766
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRX
}}{{omim
|id=605725
|rsnum=104894706
|variant=0005
}}{{ClinVar
|rsid=104894706
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=40903673
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PRX:57716
|GENE_NAME=PRX
|GENE_ID=57716
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.40903673G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605725.0005
|CLNSIG=5
|CLNCUI=CN069172; C0011195
|CLNDBN=Charcot-Marie-Tooth disease, type IVF; Dejerine-Sottas disease
|Disease=Charcot-Marie-Tooth disease; Dejerine-Sottas disease
|CLNACC=RCV000005057.1; RCV000005058.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1358:NBK1468:CN068842:614895:99952; NBK1205:NBK1468:C0011195:145900:64748:111499002
}}