{{Rsnum
|rsid=11216185
|Gene=SIK3
|Chromosome=11
|position=116912258
|Orientation=plus
|GMAF=0.07897
|Gene_s=SIK3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 0.9 | 8.0 | 91.1
| HCB | 0.0 | 13.1 | 86.9
| JPT | 0.0 | 23.9 | 76.1
| YRI | 2.0 | 21.8 | 76.2
| ASW | 0.0 | 19.3 | 80.7
| CHB | 0.0 | 13.1 | 86.9
| CHD | 0.0 | 18.3 | 81.7
| GIH | 0.0 | 13.9 | 86.1
| LWK | 0.9 | 20.0 | 79.1
| MEX | 0.0 | 10.3 | 89.7
| MKK | 0.6 | 16.7 | 82.7
| TSI | 1.0 | 9.8 | 89.2
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22306654
|Trait=None
|Title=Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis.
|RiskAllele=G
|Pval=1E-7
|OR=1.5700
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}