{{Rsnum
|rsid=60284988
|Chromosome=7
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC26A4
|position=107660756
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LOC286002,SLC26A4
}}{{omim
|id=605646
|rsnum=60284988
|variant=0027
}}

{{ClinVar
|rsid=60284988
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=107301201
|CHROM=7
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=SLC26A4-AS1:286002; SLC26A4:5172
|GENE_NAME=SLC26A4-AS1; SLC26A4
|GENE_ID=286002; 5172
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.107301201T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605646.0027
|CLNSIG=5
|CLNCUI=C0271829; C1863752
|CLNDBN=Pendred's syndrome; Enlarged vestibular aqueduct syndrome
|Disease=Pendred's syndrome; Enlarged vestibular aqueduct syndrome
|CLNACC=RCV000005109.1; RCV000005110.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:NBK1467:C0271829:274600:705:70348004; NBK1434:NBK1467:C1863752:600791:90636
}}

{{PMID|17503324|OA=1
}} Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4).

{{PMID|19204907|OA=1
}} Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?

{{PMID|19787632}} The c.-103T>C variant in the 5'-UTR of SLC26A4 gene: a pathogenic mutation or coincidental polymorphism?

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}