{{Rsnum
|rsid=121908134
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=ESPN
|position=6451926
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ESPN
}}{{omim
|id=606351
|rsnum=121908134
|variant=0003
}}{{ClinVar
|rsid=121908134
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=6451926
|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.6451926A>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000004670.1
|CLNDBN=Deafness, without vestibular involvement, autosomal dominant
|CLNSRC=ClinVar; OMIM Allelic Variant
|Disease=Deafness
|CLNSRCID=NM_031475.2:c.2155A>C; 606351.0003
}}