{{Rsnum
|rsid=211694397
|Chromosome=14
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=ESR2
|position=64235081
|Gene_s=ESR2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=14
|CLNACC=RCV000007927.2
|CLNALLE=1
|CLNDBN=Deafness, autosomal recessive 35
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1837857:608565:90636
|CLNHGVS=NC_000014.8:g.64701799G>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602167.0001
|Disease=Deafness
|FwdALT=A
|FwdREF=C
|GENEINFO=ESR2:2100
|GENE_ID=2100
|GENE_NAME=ESR2
|REF=G
|RSPOS=64701799
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=211694397
}}