{{Rsnum
|rsid=2269372
|Gene=RENBP
|Chromosome=X
|position=153942092
|Orientation=plus
|GMAF=0.494
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=RENBP
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 69.2 | 12.3 | 18.5
| HCB | 11.1 | 13.3 | 75.6
| JPT | 9.1 | 22.7 | 68.2
| YRI | 22.2 | 19.0 | 58.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 11.1 | 13.3 | 75.6
| 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=20486282
|Title=Genetic variants in the renin-angiotensin-aldosterone system and salt sensitivity of blood pressure
|OA=1
}}

{{PMID Auto
|PMID=18520591
|Title=Sequence variants in host cell factor C1 are associated with Meniere's disease.
|OA=1
}}

{{PMID Auto
|PMID=24043878
|Title=Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese
}}

{{on chip | Illumina Human 1M}}