{{Rsnum
|rsid=10989019
|Gene=INVS
|Chromosome=9
|position=100214259
|Orientation=plus
|GMAF=0.1612
|Gene_s=INVS
|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 | 0.9 | 16.8 | 82.3
| HCB | 0.0 | 1.5 | 98.5
| JPT | 0.0 | 0.0 | 100.0
| YRI | 27.9 | 45.7 | 26.4
| ASW | 21.4 | 33.9 | 44.6
| CHB | 0.0 | 1.5 | 98.5
| CHD | 0.0 | 0.9 | 99.1
| GIH | 0.0 | 5.9 | 94.1
| LWK | 24.5 | 56.4 | 19.1
| MEX | 0.0 | 5.2 | 94.8
| MKK | 7.1 | 41.0 | 51.9
| TSI | 2.0 | 15.7 | 82.4
| 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=3.21
  |ORtxt=[1.98-5.20]
  }}

{{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}}