{{Rsnum
|rsid=121908145
|Gene=BSND
|Chromosome=1
|position=54999196
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=BSND
}}{{omim
|id=606412
|rsnum=121908145
|variant=0010
}}{{ClinVar
|rsid=121908145
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=54999196
|CHROM=1
|GMAF=0.0005
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060020e05000016110100
|GENEINFO=BSND:7809
|GENE_NAME=BSND
|GENE_ID=7809
|WGT=1
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000001.11:g.54999196G>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;NSM;NSN;REF;R5;ASP;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591; .
|CLNACC=RCV000004639.1
|CLNDBN=Sensorineural deafness with mild renal dysfunction
|CLNDSDB=MedGen
|CLNDSDBID=C2748440
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_057176.2:c.10G>T; 606412.0010
|COMMON=0
|Disease=Sensorineural deafness with mild renal dysfunction
}}