{{Rsnum
|rsid=1036935
|Chromosome=18
|position=47843534
|Orientation=plus
|GMAF=0.1896
|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 | 63.7 | 31.0 | 5.3
| HCB | 89.8 | 9.5 | 0.7
| JPT | 92.0 | 7.1 | 0.9
| YRI | 44.2 | 43.5 | 12.2
| ASW | 50.9 | 40.4 | 8.8
| CHB | 89.8 | 9.5 | 0.7
| CHD | 75.2 | 23.9 | 0.9
| GIH | 59.4 | 31.7 | 8.9
| LWK | 50.9 | 39.1 | 10.0
| MEX | 77.6 | 20.7 | 1.7
| MKK | 55.8 | 40.4 | 3.8
| TSI | 61.8 | 32.4 | 5.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20062064
|Trait=Chronic lymphocytic leukemia
|Title=Common variants at 2q37.3, 8q24.21, 15q21.3 abd 16q24.1 influence chronic lymphocytic leukemia risk
|RiskAllele=T
|Pval=0.000002
|OR=1.22
|ORtxt=[1.12-1.32]
}}

{{PMID Auto
|PMID=21554262
|Title=Common genetic variation at 15q25.2 impacts on chronic lymphocytic leukaemia risk.
}}

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