{{Rsnum
|rsid=121909260
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=CASR
|position=122257275
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CASR
}}{{omim
|id=601199
|rsnum=121909260
|variant=0004
}}{{ClinVar
|rsid=121909260
|Reversed=0
|FwdREF=A
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=121976122
|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; 2
|CLNHGVS=NC_000003.11:g.121976122A>C; NC_000003.11:g.121976122A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601199.0004
|CLNSIG=5
|CLNCUI=C1832648
|CLNDBN=Hypocalcemia, autosomal dominant 1; Hypocalciuric hypercalcemia, familial, type 1
|Disease=Hypocalcemia; Hypocalciuric hypercalcemia
|CLNACC=RCV000008815.3; RCV000029450.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=C0342345:601198:2238; C0342637
}}