{{Rsnum
|rsid=5934505
|Chromosome=X
|position=8945785
|Orientation=plus
|GMAF=0.2703
|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 | 16.9 | 15.4 | 67.7
| HCB | 15.6 | 13.3 | 71.1
| JPT | 27.3 | 15.9 | 56.8
| YRI | 9.5 | 27.0 | 63.5
| ASW | 0.0 | 0.0 | 0.0
| CHB | 15.6 | 13.3 | 71.1
| CHD | 13.5 | 8.7 | 77.9
| 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|21998597|OA=1
}} "Genetic determinants of serum testosterone concentrations in men" - The rs5934505 polymorphism near FAM9B on the X chromosome was also associated with testosterone concentrations (p?=?5.6×10(-16)). The mean serum testosterone and calculated free testosterone but not SHBG concentrations were lower in men with T genotype than in those with C genotype for rs5934505.

{{PMID Auto GWAS
  |PMID=22936694
  |Trait=Androgen levels
  |Title=Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men.
  |RiskAllele=G
  |Pval=2E-8
  |OR=.09
  |ORtxt=[0.060-0.122] unit increase
  |OA=1
}}

{{PMID Auto
|PMID=23258625
|Title=Mendelian randomization suggests non-causal associations of testosterone with cardiometabolic risk factors and mortality.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}