{{Rsnum
|rsid=804280
|Gene=GATA4
|Chromosome=8
|position=11755189
|Orientation=minus
|GMAF=0.2989
|Gene_s=GATA4
|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 | 21.4 | 54.5 | 24.1
| HCB | 0.0 | 4.5 | 95.5
| JPT | 0.9 | 6.2 | 92.9
| YRI | 17.0 | 53.7 | 29.3
| ASW | 10.5 | 56.1 | 33.3
| CHB | 0.0 | 4.5 | 95.5
| CHD | 0.0 | 5.6 | 94.4
| GIH | 5.0 | 19.8 | 75.2
| LWK | 16.4 | 42.7 | 40.9
| MEX | 10.3 | 25.9 | 63.8
| MKK | 8.4 | 47.1 | 44.5
| TSI | 19.6 | 51.0 | 29.4
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23049088
  |Trait=Myopia (pathological)
  |Title=A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population.
  |RiskAllele=
  |Pval=4E-6
  |OR=NR
  |ORtxt=NR
  }}

{{PMID Auto
|PMID=17592645
|Title=Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD).
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}