{{Rsnum
|rsid=12641856
|Chromosome=4
|position=181688712
|Orientation=plus
|GMAF=0.05739
|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 | 13.3 | 85.0
| HCB | 1.5 | 8.0 | 90.5
| JPT | 0.0 | 17.7 | 82.3
| YRI | 0.0 | 0.7 | 99.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 1.5 | 8.0 | 90.5
| CHD | 0.0 | 11.9 | 88.1
| GIH | 4.0 | 26.7 | 69.3
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 10.3 | 89.7
| MKK | 0.0 | 1.3 | 98.7
| TSI | 0.0 | 13.7 | 86.3
| 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=15.19
  |ORtxt=[4.98-46.35]
  }}

{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}