{{Rsnum
|rsid=4826508
|Gene=RNF11P2
|Chromosome=X
|position=56785262
|Orientation=plus
|GMAF=0.3089
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=LOC550643
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 26.7 | 20.0 | 53.3
| JPT | 20.5 | 18.2 | 61.4
| YRI | 36.5 | 27.0 | 36.5
| ASW | 0.0 | 0.0 | 0.0
| CHB | 26.7 | 20.0 | 53.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 19.8 | 7.3 | 72.9
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23720494
  |Trait=Blood trace element (Zn levels)
  |Title=Genome-wide association study identifies loci affecting blood copper, selenium and zinc.
  |RiskAllele=T
  |Pval=1E-12
  |OR=.21
  |ORtxt=[0.15-0.27] unit increase
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}