{{Rsnum
|rsid=1867082
|Gene=RNU3P3
|Chromosome=14
|position=85270825
|Orientation=minus
|GMAF=0.4587
|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 | 34.8 | 37.5 | 27.7
| HCB | 0.7 | 18.2 | 81.0
| JPT | 0.0 | 12.4 | 87.6
| YRI | 55.8 | 38.8 | 5.4
| ASW | 59.6 | 36.8 | 3.5
| CHB | 0.7 | 18.2 | 81.0
| CHD | 0.0 | 9.2 | 90.8
| GIH | 10.9 | 46.5 | 42.6
| LWK | 49.1 | 45.5 | 5.5
| MEX | 12.1 | 44.8 | 43.1
| MKK | 27.6 | 42.3 | 30.1
| TSI | 29.4 | 55.9 | 14.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23534349
  |Trait=QRS duration
  |Title=Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans.
  |RiskAllele=A
  |Pval=1E-6
  |OR=2.82
  |ORtxt=[NR] ms increase
  }}

{{PMID Auto
|PMID=17903299
|Title=A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}