{{Rsnum
|rsid=457287
|Gene=RCL1
|Chromosome=9
|position=4834394
|Orientation=plus
|GMAF=0.1433
|Gene_s=RCL1
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 1.8 | 17.7 | 80.5
| HCB | 0.0 | 1.5 | 98.5
| JPT | 0.0 | 0.0 | 100.0
| YRI | 14.3 | 51.0 | 34.7
| ASW | 3.5 | 52.6 | 43.9
| CHB | 0.0 | 1.5 | 98.5
| CHD | 0.0 | 0.0 | 0.0
| GIH | 2.0 | 20.8 | 77.2
| LWK | 13.6 | 40.0 | 46.4
| MEX | 0.0 | 25.9 | 74.1
| MKK | 7.1 | 38.5 | 54.5
| TSI | 2.9 | 27.5 | 69.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23263863
  |Trait=Platelet counts
  |Title=GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
  |RiskAllele=A
  |Pval=1E-6
  |OR=5.99
  |ORtxt=[3.55-8.42] unit decrease
  |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}}