Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

BBS10

Bardet-Biedl syndrome 10

Chromosome
12
Cytoband
12q21.2
Variants (rsID)
10

BBS10 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q21.2). Its official name is “Bardet-Biedl syndrome 10”. The reference table lists 10 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

9 reference-table entries with clinical significance.

  • rs139053702Benignsingle nucleotide variantBardet-Biedl syndrome|Bardet-Biedl syndrome 10
  • rs142863601Benignsingle nucleotide variantBardet-Biedl syndrome 1|Bardet-Biedl syndrome|Bardet-Biedl syndrome 10
  • rs139658279Conflicting interpretationssingle nucleotide variantBardet-Biedl syndrome 1|Bardet-Biedl syndrome 10|Bardet-Biedl syndrome
  • rs141521925Conflicting interpretationssingle nucleotide variantBardet-Biedl syndrome|Bardet-Biedl syndrome 10
  • rs373458861Conflicting interpretationssingle nucleotide variantBardet-Biedl syndrome
  • rs148374859Pathogenicsingle nucleotide variantBardet-Biedl syndrome 10|Bardet-Biedl syndrome
  • rs549625604PathogenicDuplicationBardet-Biedl syndrome 10|Bardet-biedl syndrome 6/10, digenic|Bardet-Biedl syndrome|Retinitis pigmentosa|Inborn genetic diseases|Bardet-Biedl syndrome 1|Retinal dystrophy
  • rs768933093Pathogenicsingle nucleotide variantInborn genetic diseases|Bardet-Biedl syndrome 10|6 conditions|Bardet-Biedl syndrome|Retinal dystrophy
  • rs886043841PathogenicMicrosatelliteBardet-Biedl syndrome 10|Bardet-Biedl syndrome

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.