{{Rsnum
|rsid=2340727
|Chromosome=1
|position=161976937
|Orientation=plus
|GMAF=0.3095
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 70.8 | 26.5 | 2.7
| HCB | 57.7 | 39.4 | 2.9
| JPT | 77.9 | 22.1 | 0.0
| YRI | 0.7 | 18.4 | 81.0
| ASW | 5.4 | 39.3 | 55.4
| CHB | 57.7 | 39.4 | 2.9
| CHD | 56.9 | 37.6 | 5.5
| GIH | 71.3 | 23.8 | 5.0
| LWK | 1.8 | 37.3 | 60.9
| MEX | 79.3 | 20.7 | 0.0
| MKK | 10.3 | 41.7 | 48.1
| TSI | 85.3 | 13.7 | 1.0
| 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=A
  |Pval=2E-23
  |OR=.02
  |ORtxt=[0.018-0.027] unit increase
  |OA=1
}}

{{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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}