{{Rsnum
|rsid=121909341
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FOXI1
|position=170108274
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FOXI1
}}{{omim
|id=601093
|rsnum=121909341
|variant=0002
}}{{ClinVar
|rsid=121909341
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=169535278
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FOXI1:2299
|GENE_NAME=FOXI1
|GENE_ID=2299
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.169535278G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601093.0002
|CLNSIG=5
|CLNCUI=C1863752; C0271829
|CLNDBN=Enlarged vestibular aqueduct syndrome; Pendred's syndrome
|Disease=Enlarged vestibular aqueduct syndrome; Pendred's syndrome
|CLNACC=RCV000008965.1; RCV000008966.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1434:NBK1467:C1863752:600791:90636; NBK1434:NBK1467:C0271829:274600:705:70348004
}}