{{Rsnum
|rsid=17787940
|Gene=WWTR1
|Chromosome=3
|position=149532802
|Orientation=plus
|GMAF=0.07025
|Gene_s=WWTR1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 17.7 | 82.3
| HCB | 0.0 | 13.9 | 86.1
| JPT | 0.9 | 16.8 | 82.3
| YRI | 0.0 | 1.4 | 98.6
| ASW | 0.0 | 3.5 | 96.5
| CHB | 0.0 | 13.9 | 86.1
| CHD | 0.0 | 14.7 | 85.3
| GIH | 0.0 | 20.8 | 79.2
| LWK | 0.0 | 2.7 | 97.3
| MEX | 0.0 | 13.8 | 86.2
| MKK | 0.0 | 6.4 | 93.6
| TSI | 2.0 | 19.6 | 78.4
| 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=3E-6
  |OR=3.17
  |ORtxt=[1.95-5.16]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}