{{Rsnum
|rsid=74315520
|Chromosome=22
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SOX10
|position=37973767
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SOX10
}}{{omim
|id=602229
|rsnum=74315520
|variant=0010
}}{{ClinVar
|rsid=74315520
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=38369774
|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.38369774G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=602229.0010
|CLNSIG=5
|CLNCUI=C2750452; CN069053
|CLNDBN=Waardenburg syndrome type 4C; Waardenburg syndrome type 2E, with neurologic involvement
|Disease=Waardenburg syndrome type 4C; Waardenburg syndrome type 2E
|CLNACC=RCV000007826.1; RCV000007827.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=C2750452:613266:897; CN069053
}}