{{Rsnum
|rsid=4657616
|Chromosome=1
|position=159001296
|Orientation=plus
|GMAF=0.348
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=IFI16
|Gene_s=IFI16
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 36.3 | 54.0 | 9.7
| HCB | 24.8 | 51.1 | 24.1
| JPT | 40.7 | 48.7 | 10.6
| YRI | 100.0 | 0.0 | 0.0
| ASW | 78.9 | 21.1 | 0.0
| CHB | 24.8 | 51.1 | 24.1
| CHD | 25.7 | 50.5 | 23.9
| GIH | 47.5 | 41.6 | 10.9
| LWK | 99.1 | 0.9 | 0.0
| MEX | 24.1 | 36.2 | 39.7
| MKK | 94.2 | 5.8 | 0.0
| TSI | 34.3 | 48.0 | 17.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23263863
  |Trait=Hematology traits
  |Title=GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
  |RiskAllele=G
  |Pval=5E-47
  |OR=.06
  |ORtxt=[0.053-0.07] unit increase
  |OA=1
}}

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