{{Rsnum
|rsid=121965022
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=SLC26A1
|position=987842
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=IDUA,SLC26A1
}}{{omim
|id=252800
|rsnum=121965022
|variant=0006
}}{{ClinVar
|rsid=121965022
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=981630
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SLC26A1:10861; IDUA:3425
|GENE_NAME=SLC26A1; IDUA
|GENE_ID=10861; 3425
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.981630C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=252800.0006
|CLNSIG=5
|CLNCUI=C0086795
|CLNDBN=Hurler syndrome
|Disease=Hurler syndrome
|CLNACC=RCV000012689.13
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1162:C0086795:607014:93473
}}