{{Rsnum
|rsid=2280543
|Gene=BET1L
|Chromosome=11
|position=203788
|Orientation=plus
|GMAF=0.06979
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 92.0 | 8.0 | 0.0
| HCB | 74.5 | 24.8 | 0.7
| JPT | 78.8 | 20.4 | 0.9
| YRI | 85.0 | 14.3 | 0.7
| ASW | 91.2 | 8.8 | 0.0
| CHB | 74.5 | 24.8 | 0.7
| CHD | 74.3 | 19.3 | 6.4
| GIH | 80.2 | 19.8 | 0.0
| LWK | 90.0 | 10.0 | 0.0
| MEX | 93.1 | 6.9 | 0.0
| MKK | 84.6 | 15.4 | 0.0
| TSI | 95.1 | 4.9 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21460842
|Trait=None
|Title=A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids
|RiskAllele=G
|Pval=4E-12
|OR=1.3900
|ORtxt=[1.17-1.64]
}}

{{PMID Auto GWAS
|PMID=22286173
|Trait=None
|Title=Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA.
|RiskAllele=T
|Pval=0.000003
|OR=1.2510
|ORtxt=None
}}

{{PMID Auto
|PMID=23604678
|Title=BET1L and TNRC6B associate with uterine fibroid risk among European Americans
}}

{{PMID Auto
|PMID=23892540
|Title=Variants in BET1L and TNRC6B associate with increasing fibroid volume and fibroid type among European Americans
}}
{{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}}