{{Rsnum
|rsid=121908136
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ESPN
|position=6452092
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ESPN
}}{{omim
|id=606351
|rsnum=121908136
|variant=0005
}}{{ClinVar
|rsid=121908136
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=6452092
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=ESPN:83715
|GENE_NAME=ESPN
|GENE_ID=83715
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.6452092G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000004672.1
|CLNDBN=Deafness, without vestibular involvement, autosomal dominant
|CLNSRC=ClinVar; OMIM Allelic Variant
|Disease=Deafness
|CLNSRCID=NM_031475.2:c.2321G>A; 606351.0005
}}