{{Rsnum
|rsid=397514728
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CASR
|position=122261697
|Gene_s=CASR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,T
|CHROM=3
|CLNACC=RCV000054482.1; RCV000054481.1
|CLNALLE=1; 2
|CLNDBN=Familial benign hypercalcemia; Hypocalcemia, autosomal dominant 1
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet
|CLNDSDBID=C1809471:145980:405:190868007; C0342345:601198:2238
|CLNHGVS=NC_000003.11:g.121980544C>A; NC_000003.11:g.121980544C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601199.0051; 601199.0052
|Disease=Familial benign hypercalcemia; Hypocalcemia
|FwdALT=A,T
|FwdREF=C
|GENEINFO=CASR:846
|GENE_ID=846
|GENE_NAME=CASR
|REF=C
|RSPOS=121980544
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514728
}}