{{Rsnum
|rsid=74315518
|Chromosome=22
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=SOX10
|position=37974144
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SOX10
}}{{omim
|id=602229
|rsnum=74315518
|variant=0007
}}{{ClinVar
|rsid=74315518
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=38370151
|CHROM=22
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SOX10:6663
|GENE_NAME=SOX10
|GENE_ID=6663
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.38370151G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602229.0007
|CLNSIG=5
|CLNCUI=C1836727
|CLNDBN=Peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease
|Disease=Peripheral demyelinating neuropathy
|CLNACC=RCV000007823.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1836727:609136:163746
}}