Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

SMAD9

SMAD family member 9

Chromosome
13
Cytoband
13q13.3
Variants (rsID)
22

SMAD9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 13 (region 13q13.3). Its official name is “SMAD family member 9”. The reference table lists 22 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

2 reference-table entries with clinical significance.

  • rs78249575Conflicting interpretationssingle nucleotide variantPulmonary hypertension, primary, 2
  • rs111748421Uncertain significancesingle nucleotide variantPulmonary hypertension, primary, 2

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.