{{Rsnum
|rsid=121909111
|Chromosome=14
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=ESRRB
|position=76491683
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ESRRB
}}{{omim
|id=602167
|rsnum=121909111
|variant=0003
}}{{ClinVar
|rsid=121909111
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=76958026
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ESRRB:2103
|GENE_NAME=ESRRB
|GENE_ID=2103
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.76958026G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602167.0003
|CLNSIG=5
|CLNCUI=C1837857
|CLNDBN=Deafness, autosomal recessive 35
|Disease=Deafness
|CLNACC=RCV000007929.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1837857:608565:90636
}}