{{Rsnum
|rsid=925391
|Chromosome=X
|position=67120595
|Orientation=minus
|GMAF=0.2926
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 83.1 | 9.2 | 7.7
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| 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
}}[[23andMe]] seems to [https://www.23andme.com/you/journal/pre_baldness/overview/ consider] each A at rs925391 to have lowered men's odds of [[baldness]] by 11x. 

{{PMID|15902657|OA=1
}}  [[baldness]]
*lowest P value of 2.1×10-12 for [[rs10521339]]
*family based [[rs938059]] shows the lowest P value (4.03×10-6) (table 3)
*[[rs6152]] (P=6.66×10-10)

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