{{Rsnum
|rsid=4815879
|Gene=MCM8
|Chromosome=20
|position=5968888
|Orientation=plus
|GMAF=0.06566
|Gene_s=MCM8
|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 | 1.8 | 17.9 | 80.4
| HCB | 0.7 | 17.6 | 81.6
| JPT | 0.0 | 9.2 | 90.8
| YRI | 0.0 | 1.4 | 98.6
| ASW | 0.0 | 7.0 | 93.0
| CHB | 0.7 | 17.6 | 81.6
| CHD | 0.0 | 20.4 | 79.6
| GIH | 0.0 | 6.9 | 93.1
| LWK | 0.0 | 2.7 | 97.3
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 5.2 | 94.8
| TSI | 1.0 | 15.7 | 83.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23551011
  |Trait=Preeclampsia
  |Title=Genome-Wide Association Study of Pre-Eclampsia Detects Novel Maternal Single Nucleotide Polymorphisms and Copy-Number Variants in Subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study Cohort.
  |RiskAllele=
  |Pval=2E-6
  |OR=14.57
  |ORtxt=[4.81-44.17]
  }}

{{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}}