{{Rsnum
|rsid=2272007
|Gene=ULK4
|Chromosome=3
|position=41954644
|Orientation=minus
|GMAF=0.3026
|Gene_s=ULK4
|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 | 3.5 | 41.6 | 54.9
| HCB | 4.4 | 35.0 | 60.6
| JPT | 0.9 | 22.1 | 77.0
| YRI | 51.7 | 40.8 | 7.5
| ASW | 38.6 | 49.1 | 12.3
| CHB | 4.4 | 35.0 | 60.6
| CHD | 4.6 | 22.0 | 73.4
| GIH | 3.0 | 29.7 | 67.3
| LWK | 56.0 | 39.4 | 4.6
| MEX | 0.0 | 31.0 | 69.0
| MKK | 64.7 | 29.5 | 5.8
| TSI | 2.0 | 39.2 | 58.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23502783
  |Trait=Multiple myeloma (hyperdiploidy)
  |Title=The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
  |RiskAllele=A
  |Pval=2E-9
  |OR=1.47
  |ORtxt=[1.30-1.67]
  }}

{{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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}