{{Rsnum
|rsid=1394205
|Gene=FSHR
|Chromosome=2
|position=49154446
|Orientation=minus
|GMAF=0.3604
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=FSHR
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 10.6 | 38.1 | 51.3
| HCB | 24.1 | 53.3 | 22.6
| JPT | 23.0 | 48.7 | 28.3
| YRI | 6.8 | 34.7 | 58.5
| ASW | 7.0 | 43.9 | 49.1
| CHB | 24.1 | 53.3 | 22.6
| CHD | 19.4 | 52.8 | 27.8
| GIH | 6.9 | 49.5 | 43.6
| LWK | 10.1 | 43.1 | 46.8
| MEX | 27.6 | 46.6 | 25.9
| MKK | 7.7 | 47.7 | 44.5
| TSI | 8.8 | 39.2 | 52.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20335500
|Title=FSHR gene polymorphisms influence bone mineral density and bone turnover in postmenopausal women
}}

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

{{PMID Auto
|PMID=18413494
|Title=Hereditary determinants of human hypertension: strategies in the setting of genetic complexity.
|OA=1
}}

{{PMID Auto
|PMID=22414334
|Title=Follicle stimulating hormone receptor G-29A, 919A>G, 2039A>G polymorphism and the risk of male infertility: a meta-analysis.
}}

{{PMID Auto
|PMID=25052309
|Title=The FSHB -211G&gt;T variant attenuates serum FSH levels in the supraphysiological gonadotropin setting of Klinefelter syndrome
}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}