{{Rsnum
|rsid=121908362
|Gene=SLC26A4
|Chromosome=7
|position=107710132
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SLC26A4
}}{{omim
|id=605646
|rsnum=121908362
|variant=0011
}}{{ClinVar
|rsid=121908362
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=107350577
|CHROM=7
|GMAF=0.0009
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000016110100
|GENEINFO=SLC26A4:5172
|GENE_NAME=SLC26A4
|GENE_ID=5172
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.107350577A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1467; 605646.0011
|CLNSIG=5
|CLNCUI=C1863752; C0271829
|CLNDBN=Enlarged vestibular aqueduct syndrome; Pendred's syndrome; Hereditary hearing loss and deafness
|Disease=Enlarged vestibular aqueduct syndrome; Pendred's syndrome; Hereditary hearing loss and deafness
|CLNACC=RCV000005094.2; RCV000005095.1; RCV000036477.1
|Tags=PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1434:NBK1467:C1863752:600791:90636; NBK1434:NBK1467:C0271829:274600:705:70348004; NBK1434:C0236038:95827002
|COMMON=0
}}