Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

BBS9

Bardet-Biedl syndrome 9

Chromosome
7
Cytoband
7p14.3
Variants (rsID)
109

BBS9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7p14.3). Its official name is “Bardet-Biedl syndrome 9”. The reference table lists 109 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

11 reference-table entries with clinical significance.

  • rs117543061Benignsingle nucleotide variantBardet-Biedl syndrome|Bardet-Biedl syndrome 9
  • rs146752751Benignsingle nucleotide variantBardet-Biedl syndrome 1|Bardet-Biedl syndrome|Bardet-Biedl syndrome 9
  • rs34218557Benignsingle nucleotide variantBardet-Biedl syndrome|Bardet-Biedl syndrome 1|Bardet-Biedl syndrome 9
  • rs59252892Benignsingle nucleotide variantBardet-Biedl syndrome|Bardet-Biedl syndrome 9
  • rs138072724Conflicting interpretationssingle nucleotide variantBardet-Biedl syndrome|Bardet-Biedl syndrome 9
  • rs142434516Conflicting interpretationssingle nucleotide variantBardet-Biedl syndrome
  • rs145007686Conflicting interpretationssingle nucleotide variantBardet-Biedl syndrome
  • rs61753526Conflicting interpretationssingle nucleotide variantBardet-Biedl syndrome|Bardet-Biedl syndrome 9
  • rs61753527Conflicting interpretationssingle nucleotide variantBardet-Biedl syndrome|Bardet-Biedl syndrome 9
  • rs140882212Uncertain significancesingle nucleotide variantBardet-Biedl syndrome
  • rs149668719Uncertain significancesingle nucleotide variantBardet-Biedl syndrome|Bardet-Biedl syndrome 9

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.