{{Rsnum
|rsid=121965020
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC26A1
|position=987858
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=IDUA,SLC26A1
}}{{omim
|id=252800
|rsnum=121965020
|variant=0002
}}{{ClinVar
|rsid=121965020
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=981646
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000040002110100
|GENEINFO=SLC26A1:10861; IDUA:3425
|GENE_NAME=SLC26A1; IDUA
|GENE_ID=10861; 3425
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.981646C>T
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=1101; 252800.0002
|CLNSIG=5
|CLNCUI=C0086795
|CLNDBN=Hurler syndrome; not provided
|Disease=Hurler syndrome; not provided
|CLNACC=RCV000012684.21; RCV000078386.1
|Tags=PM;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1162:C0086795:607014:93473
}}