{{Rsnum
|rsid=2268361
|Gene=FSHR
|Chromosome=2
|position=48974473
|Orientation=minus
|GMAF=0.4959
|Gene_s=FSHR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 46.9 | 46.0 | 7.1
| HCB | 21.2 | 48.9 | 29.9
| JPT | 28.3 | 44.2 | 27.4
| YRI | 5.4 | 32.0 | 62.6
| ASW | 12.3 | 42.1 | 45.6
| CHB | 21.2 | 48.9 | 29.9
| CHD | 25.7 | 50.5 | 23.9
| GIH | 24.8 | 53.5 | 21.8
| LWK | 5.5 | 30.0 | 64.5
| MEX | 51.7 | 36.2 | 12.1
| MKK | 17.9 | 46.8 | 35.3
| TSI | 33.3 | 48.0 | 18.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22885925
  |Trait=Polycystic ovary syndrome
  |Title=Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome.
  |RiskAllele=C
  |Pval=1E-12
  |OR=1.15
  |ORtxt=[NR]
  }}

{{PMID Auto
|PMID=16864747
|Title=Mutation of the follicle-stimulating hormone receptor gene 5'-untranslated region associated with female hypertension.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}