{{Rsnum
|rsid=6695223
|Gene=WDR63
|Chromosome=1
|position=85066028
|Orientation=plus
|GMAF=0.1685
|Gene_s=WDR63
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 1.8 | 22.1 | 76.1
| HCB | 2.9 | 35.8 | 61.3
| JPT | 6.2 | 28.6 | 65.2
| YRI | 4.1 | 37.4 | 58.5
| ASW | 8.8 | 21.1 | 70.2
| CHB | 2.9 | 35.8 | 61.3
| CHD | 6.4 | 26.6 | 67.0
| GIH | 1.0 | 17.8 | 81.2
| LWK | 6.4 | 38.2 | 55.5
| MEX | 0.0 | 12.1 | 87.9
| MKK | 7.1 | 35.9 | 57.1
| TSI | 2.9 | 34.3 | 62.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23509962
  |Trait=Venous thromboembolism (gene x gene interaction)
  |Title=A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
  |RiskAllele=T
  |Pval=5E-9
  |OR=1.86
  |ORtxt=[NR]
  |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}}