{{Rsnum
|rsid=111033256
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=SLC26A4
|position=107675060
|Gene_s=SLC26A4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033256
|Reversed=0
|FwdREF=T
|FwdALT=A
|REF=T
|ALT=A
|RSPOS=107315505
|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
|CLNHGVS=NC_000007.13:g.107315505T>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000036506.1
|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=12676893
|Title=Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.
|OA=1
}}

{{PMID Auto
|PMID=12974744
|Title=Screening the SLC26A4 gene in probands with deafness and goiter (Pendred syndrome) ascertained from a large group of students of the schools for the deaf in Turkey.
}}

{{PMID Auto
|PMID=16460646
|Title=Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population.
|OA=1
}}