{{Rsnum
|rsid=703193
|Gene=BCLAF1
|Chromosome=6
|position=136288212
|Orientation=plus
|GMAF=0.2594
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=BCLAF1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 80.5 | 19.5 | 0.0
| HCB | 73.5 | 22.8 | 3.7
| JPT | 50.4 | 44.2 | 5.3
| YRI | 15.6 | 44.2 | 40.1
| ASW | 24.6 | 50.9 | 24.6
| CHB | 73.5 | 22.8 | 3.7
| CHD | 57.8 | 38.5 | 3.7
| GIH | 69.3 | 26.7 | 4.0
| LWK | 15.5 | 46.4 | 38.2
| MEX | 81.0 | 19.0 | 0.0
| MKK | 17.9 | 55.1 | 26.9
| TSI | 66.7 | 31.4 | 2.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20855536
|Title=Germline Variation in Apoptosis Pathway Genes and Risk of non-Hodgkin Lymphoma
|OA=1
}}

{{PMID Auto
|PMID=18043751
|Title=Admixture mapping provides evidence of association of the VNN1 gene with hypertension.
|OA=1
}}

{{PMID Auto
|PMID=20401335
|Title=Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
|OA=1
}}

{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}