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Gene entry

GNRHR

gonadotropin releasing hormone receptor

Chromosome
4
Cytoband
4q13.2
Variants (rsID)
10

GNRHR is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q13.2). Its official name is “gonadotropin releasing hormone receptor”. The reference table lists 10 variants (rsID) for this gene.

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Clinically classified variants

8 reference-table entries with clinical significance.

  • rs6552113Benignsingle nucleotide variantHypogonadotropic hypogonadism 7 with or without anosmia
  • rs104893843Likely pathogenicsingle nucleotide variantHypogonadotropic hypogonadism 7 with or without anosmia|Isolated GnRH Deficiency
  • rs104893836Pathogenicsingle nucleotide variantHypogonadotropic hypogonadism 7 with or without anosmia|Isolated congenital hypogonadotropic hypogonadism|Gonadotropin deficiency|Infertility
  • rs104893837Pathogenicsingle nucleotide variantHypogonadotropic hypogonadism 7 with or without anosmia|Amenorrhea|Hypogonadotropic hypogonadism
  • rs104893838Pathogenicsingle nucleotide variantHypogonadotropic hypogonadism 7 with or without anosmia
  • rs104893842Pathogenicsingle nucleotide variantHypogonadotropic hypogonadism 7 with or without anosmia
  • rs104893844Pathogenicsingle nucleotide variantHypogonadotropic hypogonadism 7 with or without anosmia
  • rs28933074Pathogenicsingle nucleotide variantHypogonadotropic hypogonadism 7 with or without anosmia

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.