{{Rsnum
|rsid=1531070
|Gene=MAML3
|Chromosome=4
|position=139874173
|Orientation=plus
|GMAF=0.2507
|Gene_s=MAML3
|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 | 13.3 | 55.8 | 31.0
| HCB | 2.2 | 27.9 | 69.9
| JPT | 0.9 | 21.4 | 77.7
| YRI | 1.4 | 9.6 | 89.0
| ASW | 1.8 | 17.5 | 80.7
| CHB | 2.2 | 27.9 | 69.9
| CHD | 3.7 | 16.5 | 79.8
| GIH | 5.0 | 44.6 | 50.5
| LWK | 0.0 | 6.4 | 93.6
| MEX | 6.9 | 27.6 | 65.5
| MKK | 0.0 | 6.5 | 93.5
| TSI | 11.9 | 45.5 | 42.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23708190
  |Trait=Congenital heart malformation
  |Title=A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations.
  |RiskAllele=A
  |Pval=5E-12
  |OR=1.40
  |ORtxt=[1.27-1.54]
  }}

{{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}}