{{Rsnum
|rsid=1052501
|Gene=ULK4
|Chromosome=3
|position=41883906
|Orientation=minus
|GMAF=0.2934
|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 | 54.9 | 41.6 | 3.5
| HCB | 61.3 | 32.8 | 5.8
| JPT | 77.0 | 22.1 | 0.9
| YRI | 10.9 | 40.8 | 48.3
| ASW | 12.3 | 52.6 | 35.1
| CHB | 61.3 | 32.8 | 5.8
| CHD | 74.3 | 21.1 | 4.6
| GIH | 67.3 | 29.7 | 3.0
| LWK | 6.4 | 39.1 | 54.5
| MEX | 72.4 | 27.6 | 0.0
| MKK | 5.4 | 33.6 | 61.1
| TSI | 59.4 | 38.6 | 2.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22120009
|Trait=None
|Title=Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
|RiskAllele=G
|Pval=2E-8
|OR=1.3200
|ORtxt=None
}}

{{GET Evidence
|gene=ULK4
|aa_change=Ala542Thr
|aa_change_short=A542T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1052501
|overall_frequency_n=6656
|overall_frequency_d=9734
|overall_frequency=0.683789
|n_genomes=42
|n_genomes_annotated=0
|n_haplomes=65
|n_articles=0
|n_articles_annotated=0
|nblosum100=1
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=24449210
|Title=Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
}}

{{PMID Auto
|PMID=22945773
|Title=Single-nucleotide polymorphism rs1052501 associated with monoclonal gammopathy of undetermined significance and multiple myeloma.
|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}}