{{Rsnum
|rsid=121909267
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CASR
|position=122257288
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CASR
}}{{omim
|id=601199
|rsnum=121909267
|variant=0035
}}{{ClinVar
|rsid=121909267
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=121976135
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CASR:846
|GENE_NAME=CASR
|GENE_ID=846
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.121976135C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601199.0035
|CLNSIG=5
|CLNCUI=C1832612
|CLNDBN=Hypocalcemia, autosomal dominant 1, with bartter syndrome
|Disease=Hypocalcemia
|CLNACC=RCV000008849.3
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=CN178679
}}