{{Rsnum
|rsid=2236405
|Gene=PTCH1
|Chromosome=9
|position=95449290
|Orientation=plus
|GMAF=0.07943
|Gene_s=PTCH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 2.3 | 22.7 | 75.0
| JPT | 2.3 | 23.3 | 74.4
| YRI | 3.3 | 27.9 | 68.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 2.3 | 22.7 | 75.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=24073265
|Title=Common Genetic Variations in Patched1 (PTCH1) Gene and Risk of Hirschsprung Disease in the Han Chinese Population
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}