Gene entry
FSHR
follicle stimulating hormone receptor
- Chromosome
- 2
- Cytoband
- 2p16.3
- Variants (rsID)
- 53
FSHR is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p16.3). Its official name is “follicle stimulating hormone receptor”. The reference table lists 53 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs6166Benignsingle nucleotide variantOvarian hyperstimulation syndrome|Ovarian dysgenesis 1
- rs121909659Conflicting interpretationssingle nucleotide variantOvarian dysgenesis 1|Ovarian hyperstimulation syndrome
- rs386833510Likely pathogenicsingle nucleotide variantOvarian dysgenesis 1
- rs121909658Pathogenicsingle nucleotide variantOvarian dysgenesis 1
- rs121909661Pathogenicsingle nucleotide variantOvarian dysgenesis 1
- rs121909664Pathogenicsingle nucleotide variantOvarian hyperstimulation syndrome
- rs28928870Pathogenicsingle nucleotide variantOvarian hyperstimulation syndrome
Other listed variants
- rs905668
- rs1394203
- rs1504178
- rs1553474
- rs1553476
- rs1922469
- rs1922482
- rs2091787
- rs2268361
- rs2268363
- rs2300439
- rs4140979
- rs4246578
- rs4387843
- rs4420736
- rs6545087
- rs6545091
- rs6705106
- rs6746533
- rs6760036
- rs7559066
- rs7590213
- rs7599310
- rs10185242
- rs10432668
- rs10865237
- rs11125211
- rs12613782
- rs12713034
- rs12997223
- rs17038169
- rs17824954
- rs68020305
- rs72827284
- rs77698912
- rs78234109
- rs78784563
- rs79621145
- rs79917868
- rs79978310
- rs113301654
- rs115639420
- rs116630450
- rs117277174
- rs138579337
- rs149153548
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.