{{Rsnum
|rsid=7651039
|Gene=BTD
|Chromosome=3
|position=15606497
|Orientation=plus
|GMAF=0.3609
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=BTD
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 20.4 | 53.1 | 26.5
| HCB | 36.1 | 48.9 | 15.0
| JPT | 48.6 | 40.5 | 10.8
| YRI | 82.4 | 16.2 | 1.4
| ASW | 70.2 | 28.1 | 1.8
| CHB | 36.1 | 48.9 | 15.0
| CHD | 51.0 | 41.3 | 7.7
| GIH | 18.0 | 58.0 | 24.0
| LWK | 78.5 | 21.5 | 0.0
| MEX | 32.1 | 44.6 | 23.2
| MKK | 59.1 | 37.0 | 3.9
| TSI | 34.0 | 42.0 | 24.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21378990
|Trait=None
|Title=Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
|RiskAllele=C
|Pval=0.000002
|OR=1.0600
|ORtxt=[1.04-1.09]
|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 | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}