{{Rsnum
|rsid=6052699
|Gene=RPS4XP2
|Chromosome=20
|position=4631231
|Orientation=plus
|GMAF=0.404
|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 | 27.0 | 51.4 | 21.6
| HCB | 29.4 | 52.2 | 18.4
| JPT | 21.2 | 46.0 | 32.7
| YRI | 70.5 | 27.4 | 2.1
| ASW | 54.4 | 36.8 | 8.8
| CHB | 29.4 | 52.2 | 18.4
| CHD | 25.9 | 51.9 | 22.2
| GIH | 16.8 | 55.4 | 27.7
| LWK | 73.6 | 25.5 | 0.9
| MEX | 39.7 | 41.4 | 19.0
| MKK | 61.5 | 34.0 | 4.5
| TSI | 22.8 | 52.5 | 24.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20526338
|Trait=Platelet aggregation
|Title=Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response
to agonists
|RiskAllele=A
|Pval=0.000002
|OR=None
|ORtxt=None
|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}}