{{Rsnum
|rsid=111033220
|Chromosome=7
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC26A4
|position=107690203
|Gene_s=SLC26A4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033220
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=107330648
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050068000000040002100100
|GENEINFO=SLC26A4:5172
|GENE_NAME=SLC26A4
|GENE_ID=5172
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.107330648C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;VLD;OTHERKG;LSD
|CLNACC=RCV000036430.1
|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=119323
|Title=Effect of mannitol on the traumatized spinal cord. Microangiography, blood flow patterns, and electrophysiology.
}}

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

{{PMID Auto
|PMID=10700480
|Title=Enlarged vestibular aqueduct: a radiological marker of pendred syndrome, and mutation of the PDS gene.
}}

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

{{PMID Auto
|PMID=11919333
|Title=Differential diagnosis between Pendred and pseudo-Pendred syndromes: clinical, radiologic, and molecular studies.
}}

{{PMID Auto
|PMID=15355436
|Title=Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity.
}}