{{Rsnum
|rsid=104893717
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CASR
|position=122254227
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CASR
}}{{omim
|id=601199
|rsnum=104893717
|variant=0044
}}{{ClinVar
|rsid=104893717
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=121973074
|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.121973074T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601199.0044
|CLNSIG=5
|CLNCUI=CN069155
|CLNDBN=Familial benign hypercalcemia
|Disease=Familial benign hypercalcemia
|CLNACC=RCV000008858.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1809471:145980:405:190868007
}}