{{Rsnum
|rsid=10521339
|Chromosome=X
|position=67288544
|Orientation=plus
|GMAF=0.3041
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Summary=some predictive power for baldness
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 11.1 | 20.6 | 68.3
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 100.0
| 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
}}

{{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)

{{PMID Auto
|PMID=17903294
|Title=Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}