{{Rsnum
|rsid=111033302
|Chromosome=7
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC26A4
|position=107661643
|Gene_s=LOC286002,SLC26A4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033302
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=107302088
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|GENEINFO=SLC26A4-AS1:286002; SLC26A4:5172
|GENE_NAME=SLC26A4-AS1; SLC26A4
|GENE_ID=286002; 5172
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.107302088T>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000036489.1
|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=14679580
|Title=Pendred syndrome and DFNB4-mutation screening of SLC26A4 by denaturing high-performance liquid chromatography and the identification of eleven novel mutations.
}}

{{PMID Auto
|PMID=15099345
|Title=Molecular heterogeneity in two families with auditory pigmentary syndromes: the role of neuroimaging and genetic analysis in deafness.
}}

{{PMID Auto
|PMID=16950989
|Title=Simultaneous multigene mutation detection in patients with sensorineural hearing loss through a novel diagnostic microarray: a new approach for newborn screening follow-up.
}}

{{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
}}

{{PMID Auto
|PMID=19509082
|Title=Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.
}}