{{Rsnum
|rsid=1764391
|Gene=GJA4
|Chromosome=1
|position=34795168
|Orientation=plus
|GMAF=0.3333
|Gene_s=GJA4
|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 | 45.1 | 41.6 | 13.3
| HCB | 67.9 | 29.2 | 2.9
| JPT | 69.0 | 23.0 | 8.0
| YRI | 16.4 | 47.9 | 35.6
| ASW | 22.8 | 49.1 | 28.1
| CHB | 67.9 | 29.2 | 2.9
| CHD | 70.6 | 26.6 | 2.8
| GIH | 50.5 | 45.5 | 4.0
| LWK | 28.2 | 42.7 | 29.1
| MEX | 48.3 | 48.3 | 3.4
| MKK | 21.8 | 45.5 | 32.7
| TSI | 49.0 | 45.1 | 5.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=23906684
|Title=Genetic associations with coronary heart disease: Meta-analyses of 12 candidate genetic variants
}}

{{PMID Auto
|PMID=18182569
|Title=Pharmacogenetics of minimal residual disease response in children with B-precursor acute lymphoblastic leukemia: a report from the Children's Oncology Group.
|OA=1
}}

{{PMID Auto
|PMID=22305353
|Title=Lack of association between a functional genetic variant of connexin 37 and ischemic stroke in a Taiwanese population.
}}

{{PMID Auto
|PMID=24773516
|Title=Cx37 C1019T Polymorphism May Contribute to the Pathogenesis of Coronary Heart Disease
}}

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