Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

SDCCAG8

SHH signaling and ciliogenesis regulator SDCCAG8

Chromosome
1
Cytoband
1q43-q44
Variants (rsID)
37

SDCCAG8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q43-q44). Its official name is “SHH signaling and ciliogenesis regulator SDCCAG8”. The reference table lists 37 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

7 reference-table entries with clinical significance.

  • rs10927011Benignsingle nucleotide variantBardet-Biedl syndrome 16|Senior-Loken syndrome 7|Bardet-Biedl syndrome 16|Senior-Loken syndrome 7
  • rs145877279Benignsingle nucleotide variantSenior-Loken syndrome 7|Bardet-Biedl syndrome 16|Bardet-Biedl syndrome 16|Senior-Loken syndrome 7
  • rs976529Benignsingle nucleotide variantSenior-Loken syndrome 7|Bardet-Biedl syndrome 16|Bardet-Biedl syndrome 16|Senior-Loken syndrome 7|Senior-Loken syndrome 7
  • rs118064970Conflicting interpretationssingle nucleotide variantBardet-Biedl syndrome 16|Senior-Loken syndrome 7|Senior-Loken syndrome 7|Bardet-Biedl syndrome 16
  • rs140413256Conflicting interpretationssingle nucleotide variantSenior-Loken syndrome 7|Bardet-Biedl syndrome 16|Bardet-Biedl syndrome 16|Senior-Loken syndrome 7
  • rs79762798Conflicting interpretationssingle nucleotide variantBardet-Biedl syndrome 16|Senior-Loken syndrome 7
  • rs201580075Uncertain significancesingle nucleotide variantBardet-Biedl syndrome 16|Senior-Loken syndrome 7

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.