{{Rsnum
|rsid=111033305
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC26A4
|position=107690200
|Gene_s=SLC26A4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033305
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=107330645
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|GENEINFO=SLC26A4:5172
|GENE_NAME=SLC26A4
|GENE_ID=5172
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000007.13:g.107330645G>A; NC_000007.13:g.107330645G>C
|CLNORIGIN=1
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000036428.1; RCV000036429.1
|Tags=PM;PMC;OTHERKG;LSD
|CLNDBN=Hereditary hearing loss and deafness; Pendred's syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1434:C0236038:95827002; NBK1434:NBK1467:C0271829:274600:705:70348004
|Disease=Hereditary hearing loss and deafness; Pendred's syndrome
}}{{PMID Auto
|PMID=1960865
|Title=[Angiotensin converting enzyme inhibitor].
}}

{{PMID Auto
|PMID=9618166
|Title=Two frequent missense mutations in Pendred syndrome.
}}

{{PMID Auto
|PMID=9618167
|Title=Molecular analysis of the PDS gene in Pendred syndrome.
}}

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

{{PMID Auto
|PMID=16053392
|Title=Molecular analysis of the PDS gene in a nonconsanguineous Sicilian family with Pendred's syndrome.
}}

{{PMID Auto
|PMID=17766716
|Title=High phenotypic intrafamilial variability in patients with Pendred syndrome and a novel duplication in the SLC26A4 gene: clinical characterization and functional studies of the mutated SLC26A4 protein.
}}

{{PMID Auto
|PMID=12676893
|Title=Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.
|OA=1
}}