{{Rsnum
|rsid=4665058
|Gene=BAZ2B
|Chromosome=2
|position=159333698
|Orientation=plus
|GMAF=0.1111
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=BAZ2B
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.0 | 6.2 | 93.8
| HCB | 2.2 | 20.0 | 77.8
| JPT | 2.3 | 18.2 | 79.5
| YRI | 17.5 | 39.7 | 42.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 2.2 | 20.0 | 77.8
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}[[rs4665058]] is a SNP in the bromodomain adjacent zinc finger domain 2B [[BAZ2B]] locus on ch 2q24.2.

A GWAS meta-analysis in 1,283 cases of sudden cardiac death (SCD; presumably from [[myocardial infarction]]) and >20,000 control individuals of European ancestry from 5 studies, with follow-up genotyping in 3,000+ cases, associated [[rs4665058]] with SCD risk (p = 1.8×10e?10). The per allele odds ratio for the risk allele, [[rs4665058]](A), is 1.92 (CI: 1.57–2.34).{{doi|10.1371/journal.pgen.1002158}}

{{PMID Auto GWAS
|PMID=21738491
|Trait=None
|Title=Identification of a Sudden Cardiac Death Susceptibility Locus at 2q24.2 through Genome-Wide Association in European Ancestry Individuals.
|RiskAllele=A
|Pval=2E-10
|OR=1.9200
|ORtxt=[1.57-2.34]
|OA=1
}}

{{on chip | FTDNA2}}
{{on chip | FTDNA}}