{{Rsnum
|rsid=104893709
|Chromosome=3
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CASR
|position=122257175
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CASR
}}{{omim
|id=601199
|rsnum=104893709
|variant=0042
}}{{ClinVar
|rsid=104893709
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=121976022
|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
|CLNHGVS=NC_000003.11:g.121976022G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601199.0042
|CLNSIG=5
|CLNCUI=C1832645
|CLNDBN=Hyperparathyroidism, neonatal severe
|Disease=Hyperparathyroidism
|CLNACC=RCV000008856.3
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=CN069156
}}