{{Rsnum
|rsid=1994318
|Gene=MICAL2
|Chromosome=11
|position=12138114
|Orientation=plus
|GMAF=0.4908
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=MICAL2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 51.8 | 36.6 | 11.6
| HCB | 26.5 | 49.3 | 24.3
| JPT | 26.8 | 42.0 | 31.2
| YRI | 3.4 | 41.1 | 55.5
| ASW | 10.5 | 57.9 | 31.6
| CHB | 26.5 | 49.3 | 24.3
| CHD | 24.8 | 56.0 | 19.3
| GIH | 15.8 | 46.5 | 37.6
| LWK | 11.8 | 41.8 | 46.4
| MEX | 13.8 | 50.0 | 36.2
| MKK | 15.4 | 48.1 | 36.5
| TSI | 31.4 | 57.8 | 10.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23534349
  |Trait=PR interval
  |Title=Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans.
  |RiskAllele=A
  |Pval=2E-6
  |OR=6.79
  |ORtxt=[NR] ms decrease
  }}

{{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}}