{{Rsnum
|rsid=1248993
|Chromosome=10
|position=29027223
|Orientation=plus
|GMAF=0.1111
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 80.5 | 16.8 | 2.7
| HCB | 98.5 | 1.5 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 50.3 | 40.8 | 8.8
| ASW | 64.9 | 31.6 | 3.5
| CHB | 98.5 | 1.5 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 87.1 | 12.9 | 0.0
| LWK | 55.5 | 38.2 | 6.4
| MEX | 86.2 | 13.8 | 0.0
| MKK | 48.1 | 42.3 | 9.6
| TSI | 80.4 | 17.6 | 2.0
| 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=6E-6
  |OR=4.27
  |ORtxt=[2.28-8.01]
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}