{{Rsnum
|rsid=111033244
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC26A4
|position=107690125
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC26A4
}}{{omim
|id=605646
|rsnum=111033244
|variant=0008
}}
{{omim
|id=605646
|rsnum=111033244
|variant=0026
}}{{ClinVar
|rsid=111033244
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=107330570
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=SLC26A4:5172
|GENE_NAME=SLC26A4
|GENE_ID=5172
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.107330570A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605646.0008; 605646.0026
|CLNSIG=5
|CLNCUI=C0271829
|CLNDBN=Pendred's syndrome; Hereditary hearing loss and deafness
|Disease=Pendred's syndrome; Hereditary hearing loss and deafness
|CLNACC=RCV000005089.1; RCV000036425.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1434:NBK1467:C0271829:274600:705:70348004; NBK1434:C0236038:95827002
}}{{PMID Auto
|PMID=183102
|Title=[Reaction capabilities and structure of poly(rG) and poly(rG)-poly(rC) in solution by the method of the kinetics of hydrogen ion exchange].
}}

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

{{PMID Auto
|PMID=12788906
|Title=Mutations in the PDS gene in German families with Pendred's syndrome: V138F is a founder mutation.
}}

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

{{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=15689455
|Title=SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities.
|OA=1
}}