{{Rsnum
|rsid=17412740
|Chromosome=8
|position=20389247
|Orientation=plus
|GMAF=0.05647
|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 | 0.9 | 14.2 | 85.0
| HCB | 2.2 | 21.9 | 75.9
| JPT | 1.8 | 17.7 | 80.5
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 1.8 | 98.2
| CHB | 2.2 | 21.9 | 75.9
| CHD | 0.0 | 23.9 | 76.1
| GIH | 0.0 | 5.9 | 94.1
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 10.3 | 89.7
| MKK | 0.0 | 0.0 | 0.0
| TSI | 1.0 | 19.6 | 79.4
| 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=6.08
  |ORtxt=[2.88-12.81]
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}