{{Rsnum
|rsid=111033205
|Chromosome=7
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SLC26A4
|position=107661726
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LOC286002,SLC26A4
}}{{omim
|id=605646
|rsnum=111033205
|variant=0028
}}{{ClinVar
|rsid=111033205
|Reversed=0
|FwdREF=G
|FwdALT=C,T
|REF=G
|ALT=C,T
|RSPOS=107302171
|CHROM=7
|dbSNPBuildID=132
|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; 2
|CLNHGVS=NC_000007.13:g.107302171G>C; NC_000007.13:g.107302171G>T
|CLNORIGIN=1
|CLNSRCID=
605646.0028
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000005111.1; RCV000036509.1; RCV000036510.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDBN=Enlarged vestibular aqueduct syndrome; Hereditary hearing loss and deafness; Pendred's syndrome
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1434:NBK1467:C1863752:600791:90636; NBK1434:C0236038:95827002; NBK1434:NBK1467:C0271829:274600:705:70348004
|CLNSRC=OMIM Allelic Variant
|Disease=Enlarged vestibular aqueduct syndrome; Hereditary hearing loss and deafness; Pendred's syndrome
}}{{PMID|11317356}} Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations.

{{PMID|14679580}} Pendred syndrome and DFNB4-mutation screening of SLC26A4 by denaturing high-performance liquid chromatography and the identification of eleven novel mutations.

{{PMID|15355436}} Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity.