{{Rsnum
|rsid=121434605
|Chromosome=3
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=PTH1R
|position=46898112
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTH1R
}}{{omim
|id=168468
|rsnum=121434605
|variant=0014
}}{{ClinVar
|rsid=121434605
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=46939602
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PTH1R:5745
|GENE_NAME=PTH1R
|GENE_ID=5745
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.46939602G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=168468.0014
|CLNSIG=5
|CLNCUI=C1852222
|CLNDBN=Failure of tooth eruption, primary
|Disease=Failure of tooth eruption
|CLNACC=RCV000014761.24
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1852222:125350
}}