{{Rsnum
|rsid=111033317
|Chromosome=7
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=SLC26A4
|position=107698045
|Gene_s=SLC26A4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033317
|Reversed=0
|FwdALT=C
|REF=T
|ALT=TC
|RSPOS=107338490
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002100200
|GENEINFO=SLC26A4:5172
|GENE_NAME=SLC26A4
|GENE_ID=5172
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.107338490_107338491insC
|CLNORIGIN=1
|CLNSIG=4
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000036448.1
|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
}}