{{Rsnum
|rsid=29784
|Chromosome=5
|position=173168305
|Orientation=minus
|GMAF=0.3512
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 20.4 | 53.1 | 26.5
| HCB | 2.2 | 32.8 | 65.0
| JPT | 0.0 | 21.2 | 78.8
| YRI | 8.8 | 38.1 | 53.1
| ASW | 15.8 | 35.1 | 49.1
| CHB | 2.2 | 32.8 | 65.0
| CHD | 1.8 | 32.1 | 66.1
| GIH | 1.0 | 29.7 | 69.3
| LWK | 9.1 | 36.4 | 54.5
| MEX | 20.7 | 37.9 | 41.4
| MKK | 10.3 | 41.0 | 48.7
| TSI | 22.5 | 53.9 | 23.5
| HapMapRevision=28
}}{{PMID Auto
|PMID=22306654
|Title=Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis
|OA=1
}}

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