{{Rsnum
|rsid=1328369
|Gene=GPC6
|Chromosome=13
|position=93260737
|Orientation=minus
|GMAF=0.376
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=GPC6
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 28.8 | 54.1 | 17.1
| HCB | 48.5 | 39.6 | 11.9
| JPT | 51.8 | 44.6 | 3.6
| YRI | 55.5 | 39.0 | 5.5
| ASW | 31.6 | 59.6 | 8.8
| CHB | 48.5 | 39.6 | 11.9
| CHD | 45.0 | 43.1 | 11.9
| GIH | 31.7 | 43.6 | 24.8
| LWK | 35.5 | 54.5 | 10.0
| MEX | 60.3 | 34.5 | 5.2
| MKK | 35.9 | 48.7 | 15.4
| TSI | 26.5 | 53.9 | 19.6
| HapMapRevision=28
}}

{{omim
|desc=FAILURE OF TOOTH ERUPTION, PRIMARY; PFE
|id=125350
|rsnum=1328369
}}

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

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