{{Rsnum
|rsid=104893706
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=CASR
|position=122284482
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CASR
}}{{omim
|id=601199
|rsnum=104893706
|variant=0034
}}{{ClinVar
|rsid=104893706
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=122003329
|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.122003329C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601199.0034
|CLNSIG=5
|CLNCUI=C1832612; C1832648
|CLNDBN=Hypocalcemia, autosomal dominant 1, with bartter syndrome; Hypocalcemia, autosomal dominant 1
|Disease=Hypocalcemia
|CLNACC=RCV000008847.3; RCV000054480.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen; MedGen:OMIM:Orphanet
|CLNDSDBID=CN178679; C0342345:601198:2238
}}