{{Rsnum
|rsid=7988100
|Gene=NALCN
|Chromosome=13
|position=101227208
|Orientation=plus
|GMAF=0.2149
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=NALCN
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 3.5 | 20.4 | 76.1
| HCB | 17.5 | 44.5 | 38.0
| JPT | 9.7 | 38.1 | 52.2
| YRI | 0.0 | 10.2 | 89.8
| ASW | 0.0 | 17.5 | 82.5
| CHB | 17.5 | 44.5 | 38.0
| CHD | 17.4 | 45.9 | 36.7
| GIH | 6.0 | 30.0 | 64.0
| LWK | 0.0 | 5.5 | 94.5
| MEX | 12.1 | 41.4 | 46.6
| MKK | 1.3 | 19.2 | 79.5
| TSI | 4.9 | 28.4 | 66.7
| HapMapRevision=28
}}{{omim
|desc=FAILURE OF TOOTH ERUPTION, PRIMARY; PFE
|id=125350
|rsnum=7988100
}}

{{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}}