{{Rsnum
|rsid=2839440
|Gene=ZNF295-AS1
|Chromosome=21
|position=42023389
|Orientation=plus
|GMAF=0.202
|Gene_s=ZNF295-AS1
|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 | 73.5 | 23.9 | 2.7
| HCB | 48.9 | 37.2 | 13.9
| JPT | 38.9 | 50.4 | 10.6
| YRI | 74.1 | 23.1 | 2.7
| ASW | 63.2 | 33.3 | 3.5
| CHB | 48.9 | 37.2 | 13.9
| CHD | 55.6 | 38.9 | 5.6
| GIH | 83.2 | 16.8 | 0.0
| LWK | 70.9 | 26.4 | 2.7
| MEX | 79.3 | 20.7 | 0.0
| MKK | 57.8 | 37.0 | 5.2
| TSI | 66.7 | 30.4 | 2.9
| 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=1E-6
  |OR=5.31
  |ORtxt=[2.70-10.42]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}