{{Rsnum
|rsid=74315516
|Chromosome=22
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SOX10
|position=37973957
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SOX10
}}{{omim
|id=602229
|rsnum=74315516
|variant=0006
}}{{ClinVar
|rsid=74315516
|Reversed=1
|FwdREF=C
|FwdALT=A,G
|REF=G
|ALT=C,T
|RSPOS=38369964
|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.38369964G>C
|CLNORIGIN=0
|CLNSRCID=
602229.0006
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000007822.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDBN=Peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1836727:609136:163746
|CLNSRC=OMIM Allelic Variant
|Disease=Peripheral demyelinating neuropathy
}}