{{Rsnum
|rsid=111033306
|Chromosome=7
|Orientation=plus
|geno1=(-;-)
|geno2=(-;TGC)
|geno3=(TGC;TGC)
|Gene=SLC26A4
|position=107694423
|Gene_s=SLC26A4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033306
|Reversed=0
|FwdREF=TGC
|FwdALT=
|REF=CTGC
|ALT=C
|RSPOS=107334864
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050068000000000002100200
|GENEINFO=SLC26A4:5172
|GENE_NAME=SLC26A4
|GENE_ID=5172
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.107334868_107334870delTGC
|CLNORIGIN=1
|CLNSIG=4
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000036434.1
|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=14679580
|Title=Pendred syndrome and DFNB4-mutation screening of SLC26A4 by denaturing high-performance liquid chromatography and the identification of eleven novel mutations.
}}