{{Rsnum
|rsid = 28936684
|Gene = CASR
|geno1 = (G;G)
|geno2 = (G;T)
|geno3 = (T;T)
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|Chromosome=3
|position=122261715
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CASR
}}{{omim
|desc=HYPERPARATHYROIDISM, NEONATAL SEVERE PRIMARY
|id=601199
|rsnum=28936684
|variant=0006
}}

{{omim
|id=601199
|rsnum=28936684
|variant=0049
}}

{{ClinVar
|rsid=28936684
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=121980562
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CASR:846
|GENE_NAME=CASR
|GENE_ID=846
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000003.11:g.121980562G>A; NC_000003.11:g.121980562G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601199.0049; 601199.0006
|CLNSIG=5
|CLNCUI=CN069155; C1832645
|CLNDBN=Familial benign hypercalcemia; Hyperparathyroidism, neonatal severe
|Disease=Familial benign hypercalcemia; Hyperparathyroidism
|CLNACC=RCV000008863.3; RCV000008818.3
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=C1809471:145980:405:190868007; CN069156
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}