{{Rsnum
|rsid=397516418
|Chromosome=7
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=SLC26A4
|position=107694718
|Gene_s=SLC26A4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=7
|CLNACC=RCV000036442.1
|CLNALLE=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
|CLNHGVS=NC_000007.13:g.107335163T>G
|CLNSIG=5
|Disease=Hereditary hearing loss and deafness; Pendred's syndrome
|FwdALT=G
|FwdREF=T
|GENEINFO=SLC26A4:5172
|GENE_ID=5172
|GENE_NAME=SLC26A4
|REF=T
|RSPOS=107335163
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=397516418
}}