{{Rsnum
|rsid=6599175
|Gene=ULK4
|Chromosome=3
|position=41744517
|Orientation=plus
|GMAF=0.2961
|Gene_s=ULK4
|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 | 3.5 | 41.6 | 54.9
| HCB | 5.8 | 32.1 | 62.0
| JPT | 0.9 | 22.1 | 77.0
| YRI | 59.2 | 33.3 | 7.5
| ASW | 35.1 | 49.1 | 15.8
| CHB | 5.8 | 32.1 | 62.0
| CHD | 4.6 | 22.0 | 73.4
| GIH | 3.0 | 30.7 | 66.3
| LWK | 56.0 | 35.8 | 8.3
| MEX | 0.0 | 24.1 | 75.9
| MKK | 66.0 | 27.6 | 6.4
| TSI | 2.0 | 37.3 | 60.8
| 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=G
  |Pval=1E-9
  |OR=1.48
  |ORtxt=[1.30-1.68]
  }}

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