Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

HBD

hypophosphatemic bone disease

Chromosome
11
Cytoband
—
Variants (rsID)
7

HBD is a gene identifier without a current public annotation, located on chromosome 11. Its official name is “hypophosphatemic bone disease”. The reference table lists 7 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

5 reference-table entries with clinical significance.

  • rs35152987Conflicting interpretationssingle nucleotide variantdelta Thalassemia|HEMOGLOBIN A(2) YIALOUSA|Fetal hemoglobin quantitative trait locus 1
  • rs28933076Othersingle nucleotide variantHEMOGLOBIN A(2) WRENS
  • rs28933077Othersingle nucleotide variantHEMOGLOBIN A(2) SANT' ANTIOCO
  • rs35848600Othersingle nucleotide variantHEMOGLOBIN A(2) FITZROY
  • rs35849348Othersingle nucleotide variantHEMOGLOBIN A(2) BABINGA

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.