{{Rsnum
|rsid=111033309
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC26A4
|position=107702038
|Gene_s=SLC26A4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033309
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=107342483
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|GENEINFO=SLC26A4:5172
|GENE_NAME=SLC26A4
|GENE_ID=5172
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.107342483G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000036467.1
|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=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=11932316
|Title=Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome.
}}