{{Rsnum
|rsid=104893705
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CASR
|position=122283896
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CASR
}}{{omim
|id=601199
|rsnum=104893705
|variant=0032
}}{{ClinVar
|rsid=104893705
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=122002743
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CASR:846
|GENE_NAME=CASR
|GENE_ID=846
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.122002743C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601199.0032
|CLNSIG=5
|CLNCUI=C1832645
|CLNDBN=Familial benign hypercalcemia; Hyperparathyroidism, neonatal severe
|Disease=Familial benign hypercalcemia; Hyperparathyroidism
|CLNACC=RCV000008843.2; RCV000054484.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=C1809471:145980:405:190868007; CN069156
}}