{{Rsnum
|rsid=1402366
|Chromosome=3
|position=22724978
|Orientation=plus
|GMAF=0.1042
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 0.0 | 16.8 | 83.2
| HCB | 0.0 | 4.4 | 95.6
| JPT | 0.0 | 4.4 | 95.6
| YRI | 2.7 | 27.9 | 69.4
| ASW | 0.0 | 28.1 | 71.9
| CHB | 0.0 | 4.4 | 95.6
| CHD | 0.0 | 4.6 | 95.4
| GIH | 1.0 | 5.9 | 93.1
| LWK | 0.9 | 30.3 | 68.8
| MEX | 0.0 | 22.4 | 77.6
| MKK | 0.6 | 24.4 | 75.0
| TSI | 2.9 | 22.5 | 74.5
| HapMapRevision=28
}}{{omim
|desc=FAILURE OF TOOTH ERUPTION, PRIMARY; PFE
|id=125350
|rsnum=1402366
}}

{{PMID Auto
|PMID=19061984
|Title=PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}