{{Rsnum
|rsid=766325
|Gene=PAX7
|Chromosome=1
|position=18629964
|Orientation=plus
|GMAF=0.4954
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PAX7
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 33.6 | 44.2 | 22.1
| HCB | 2.2 | 23.4 | 74.5
| JPT | 1.8 | 21.2 | 77.0
| YRI | 73.5 | 23.8 | 2.7
| ASW | 56.1 | 40.4 | 3.5
| CHB | 2.2 | 23.4 | 74.5
| CHD | 2.8 | 24.1 | 73.1
| GIH | 24.8 | 43.6 | 31.7
| LWK | 64.5 | 33.6 | 1.8
| MEX | 22.4 | 53.4 | 24.1
| MKK | 54.5 | 39.7 | 5.8
| TSI | 26.5 | 53.9 | 19.6
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19142206
|Title=Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations
|OA=1
}}

{{PMID Auto
|PMID=23463464
|Title=Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}