{{Rsnum
|rsid=111033307
|Chromosome=7
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=SLC26A4
|position=107694473
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC26A4
}}{{omim
|id=605646
|rsnum=111033307
|variant=0018
}}{{ClinVar
|rsid=111033307
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=107334918
|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.107334918T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605646.0018
|CLNSIG=5
|CLNCUI=C0271829
|CLNDBN=Pendred's syndrome; Hereditary hearing loss and deafness
|Disease=Pendred's syndrome; Hereditary hearing loss and deafness
|CLNACC=RCV000005100.1; RCV000036437.1
|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=96181
|Title=Linkage between a gene for a serum protein and the gene for the Ig kappa light chain in rabbits.
}}

{{PMID Auto
|PMID=10602116
|Title=Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutation.
}}

{{PMID Auto
|PMID=11748854
|Title=Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment.
}}

{{PMID Auto
|PMID=18285825
|Title=A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and DFNB4 hearing loss.
}}

{{PMID Auto
|PMID=18813951
|Title=Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairment.
}}

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