{{Rsnum
|rsid=4545
|Gene=CYP11B2
|Chromosome=8
|position=142912625
|Orientation=minus
|GMAF=0.1538
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CYP11B2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 3.2 | 96.8
| HCB | 24.4 | 57.8 | 17.8
| JPT | 15.9 | 61.4 | 22.7
| YRI | 0.0 | 4.8 | 95.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 24.4 | 57.8 | 17.8
| 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
}}{{PMID Auto
|PMID=21127960
|Title=Haplotype-Based Case-Control Study of the Human CYP11B2 Gene and Essential Hypertension in Yi and Hani Minorities of China
}}

{{PMID Auto
|PMID=20193392
|Title=[Associations of the genetic polymorphisms in CYP11B2 gene with nonfamilial structural atrial fibrillation].
}}

{{PMID Auto
|PMID=21269059
|Title=Association of the human CYP11B2 gene and essential hypertension in southwest Han Chinese population: a haplotype-based case-control study.
}}

{{GET Evidence
|gene=CYP11B2
|aa_change=Gly435Ser
|aa_change_short=G435S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4545
|overall_frequency_n=242
|overall_frequency_d=10758
|overall_frequency=0.0224949
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.011
|genetests_testable=Y
|nblosum100=2
|autoscore=2
|n_web_uneval=4
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}