{{Rsnum
|rsid=6563695
|Chromosome=13
|position=39329106
|Orientation=plus
|GMAF=0.141
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 85.7 | 14.3 | 0.0
| HCB | 80.2 | 19.1 | 0.8
| JPT | 54.5 | 43.8 | 1.8
| YRI | 52.1 | 36.6 | 11.3
| ASW | 60.7 | 35.7 | 3.6
| CHB | 80.2 | 19.1 | 0.8
| CHD | 81.5 | 18.5 | 0.0
| GIH | 62.6 | 29.3 | 8.1
| LWK | 58.2 | 33.6 | 8.2
| MEX | 69.6 | 30.4 | 0.0
| MKK | 65.1 | 30.9 | 3.9
| TSI | 79.6 | 20.4 | 0.0
| 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=5E-6
  |OR=3.65
  |ORtxt=[2.09-6.36]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}