{{Rsnum
|rsid=7551188
|Gene=RUNX3
|Chromosome=1
|position=24946709
|Orientation=plus
|GMAF=0.4844
|Gene_s=RUNX3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 31.0 | 42.5 | 26.5
| HCB | 26.3 | 49.6 | 24.1
| JPT | 23.9 | 49.6 | 26.5
| YRI | 20.4 | 55.1 | 24.5
| ASW | 15.8 | 43.9 | 40.4
| CHB | 26.3 | 49.6 | 24.1
| CHD | 25.9 | 55.6 | 18.5
| GIH | 25.7 | 47.5 | 26.7
| LWK | 16.5 | 56.9 | 26.6
| MEX | 32.8 | 34.5 | 32.8
| MKK | 18.6 | 49.4 | 32.1
| TSI | 23.5 | 39.2 | 37.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23266558
  |Trait=Crohn's disease
  |Title=A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population.
  |RiskAllele=T
  |Pval=9E-6
  |OR=1.18
  |ORtxt=[1.10-1.28]
  }}

{{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}}