{{Rsnum
|rsid=111033254
|Chromosome=7
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC26A4
|position=107698085
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC26A4
}}{{omim
|id=605646
|rsnum=111033254
|variant=0025
}}{{ClinVar
|rsid=111033254
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=107338530
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=SLC26A4:5172
|GENE_NAME=SLC26A4
|GENE_ID=5172
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.107338530T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605646.0025
|CLNSIG=5
|CLNCUI=C0271829
|CLNDBN=Pendred's syndrome; Hereditary hearing loss and deafness
|Disease=Pendred's syndrome; Hereditary hearing loss and deafness
|CLNACC=RCV000005107.1; RCV000036449.1
|Tags=PM;PMC;S3D;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=165700
|Title=Getting it all together: coordinator for continuing care.
}}

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

{{PMID Auto
|PMID=11317356
|Title=Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations.
}}

{{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=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
}}