{{Rsnum
|rsid=17483466
|Gene=ACOXL
|Chromosome=2
|position=111039881
|Orientation=plus
|GMAF=0.118
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ACOXL
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 64.2 | 33.0 | 2.8
| HCB | 98.5 | 1.5 | 0.0
| JPT | 97.3 | 2.7 | 0.0
| YRI | 94.5 | 5.5 | 0.0
| ASW | 86.0 | 14.0 | 0.0
| CHB | 98.5 | 1.5 | 0.0
| CHD | 99.1 | 0.9 | 0.0
| GIH | 67.3 | 28.7 | 4.0
| LWK | 90.7 | 9.3 | 0.0
| MEX | 72.4 | 24.1 | 3.4
| MKK | 85.0 | 13.7 | 1.3
| TSI | 60.8 | 37.3 | 2.0
| HapMapRevision=28
}}[http://blog.23andme.com/2008/08/31/snpwatch-researchers-find-first-snps-linked-to-common-type-of-leukemia/ 23andMe blog] chronic lymphocytic [[leukemia]]
*[[rs17483466]] 	G	1.39

{{GWAS Summary
|SNP=rs17483466
|PubMedID=18758461
|Condition=Chronic lymphocytic leukemia
|Gene=ACOXL,BCL2L11
|Risk Allele=G
|pValue=2.00E-010
|OR=1.39
|95CI=1.25-1.53
}}

{{PharmGKB
|RSID=rs17483466
|Name_s=
|Gene_s=ACOXL
|Feature=
|Evidence=PubMed ID:18758461; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS Results: A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia (Initial Sample Size: 505 cases, 1,438 controls; Replication Sample Size: 1,024 cases, 1,677 controls; Risk Allele: rs17483466-G). This variant is associated with Chronic lymphocytic leukemia.
|Drugs=
|Drug Classes=
|Diseases=Leukemia; Leukemia, Lymphocytic, Chronic, B-Cell
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356375
}}

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

{{PMID|20731705|OA=1
}} Genetic susceptibility for chronic lymphocytic leukemia among Chinese in Hong Kong.

{{PMID Auto GWAS
|PMID=22700719
|Trait=None
|Title=Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
|RiskAllele=
|Pval=5E-9
|OR=1.4300
|ORtxt=None
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs17483466
|overall_frequency_n=13
|overall_frequency_d=126
|overall_frequency=0.103175
|n_genomes=13
|n_genomes_annotated=0
|n_haplomes=15
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{PMID Auto GWAS
  |PMID=23770605
  |Trait=Chronic lymphocytic leukemia
  |Title=Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
  |RiskAllele=G
  |Pval=4E-17
  |OR=1.37
  |ORtxt=[NR]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}