{{Rsnum
|rsid=104894272
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PTH
|position=13492789
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTH
}}{{omim
|id=168450
|rsnum=104894272
|variant=0003
}}{{ClinVar
|rsid=104894272
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=13514336
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PTH:5741
|GENE_NAME=PTH
|GENE_ID=5741
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.13514336A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=168450.0003
|CLNSIG=5
|CLNCUI=C1832648
|CLNDBN=Hypocalcemia, autosomal dominant
|Disease=Hypocalcemia
|CLNACC=RCV000014766.18
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1832648:146200:2238
}}