{{Rsnum
|rsid=2456449
|Chromosome=8
|position=127180736
|Orientation=plus
|GMAF=0.3228
|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 | 38.9 | 52.2 | 8.8
| HCB | 33.1 | 52.2 | 14.7
| JPT | 31.0 | 59.3 | 9.7
| YRI | 68.0 | 30.6 | 1.4
| ASW | 66.7 | 33.3 | 0.0
| CHB | 33.1 | 52.2 | 14.7
| CHD | 29.4 | 51.4 | 19.3
| GIH | 54.5 | 34.7 | 10.9
| LWK | 70.9 | 25.5 | 3.6
| MEX | 39.7 | 46.6 | 13.8
| MKK | 50.6 | 44.2 | 5.1
| TSI | 52.9 | 37.3 | 9.8
| 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=G
|Pval=8E-10
|OR=1.26
|ORtxt=[1.17-1.35]
}}

{{PMID Auto
|PMID=20855867
|Title=Inherited genetic susceptibility to monoclonal B-cell lymphocytosis
}}

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