{{Rsnum
|rsid=74315289
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=BSND
|position=54999325
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=BSND
}}{{omim
|id=606412
|rsnum=74315289
|variant=0008
}}{{ClinVar
|rsid=74315289
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=54999325
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060020a05000002110100
|GENEINFO=BSND:7809
|GENE_NAME=BSND
|GENE_ID=7809
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.54999325G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_057176.2:c.139G>A; 606412.0008
|CLNSIG=5
|CLNCUI=C1865270
|CLNDBN=Bartter syndrome type 4
|Disease=Bartter syndrome type 4
|CLNACC=RCV000004637.1
|Tags=PM;NSM;REF;R5;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1865270:602522
}}