{{Rsnum
|rsid=387907324
|Chromosome=20
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CYP24A1
|position=54162743
|Gene_s=CYP24A1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=20
|CLNACC=RCV000033211.26
|CLNALLE=1
|CLNDBN=Idiopathic hypercalcemia of infancy
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268080:143880:300547:34225008
|CLNHGVS=NC_000020.10:g.52779282C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=126065.0007
|Disease=Idiopathic hypercalcemia of infancy
|FwdALT=A
|FwdREF=G
|REF=C
|RSPOS=52779282
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907324
|GENEINFO=CYP24A1:1591
|GENE_ID=1591
|GENE_NAME=CYP24A1
}}