{{Rsnum
|rsid=121909259
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CASR
|position=122261924
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CASR
}}{{omim
|id=601199
|rsnum=121909259
|variant=0002
}}{{ClinVar
|rsid=121909259
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=121980771
|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.121980771G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601199.0002
|CLNSIG=5
|CLNCUI=CN069155; CN069156
|CLNDBN=Familial benign hypercalcemia; Hyperparathyroidism, neonatal severe
|Disease=Familial benign hypercalcemia; Hyperparathyroidism
|CLNACC=RCV000008811.2; RCV000008812.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=C1809471:145980:405:190868007; CN069156
}}