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Gene entry

ARHGAP31

Rho GTPase activating protein 31

Chromosome
3
Cytoband
3q13.32-q13.33
Variants (rsID)
36

ARHGAP31 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q13.32-q13.33). Its official name is “Rho GTPase activating protein 31”. The reference table lists 36 variants (rsID) for this gene.

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Clinically classified variants

6 reference-table entries with clinical significance.

  • rs200397968Benignsingle nucleotide variantAdams-Oliver syndrome 1
  • rs3796360Benignsingle nucleotide variantAdams-Oliver syndrome 1
  • rs61744410Benignsingle nucleotide variantAdams-Oliver syndrome 1
  • rs72960626Benignsingle nucleotide variantAdams-Oliver syndrome 1
  • rs200233879Conflicting interpretationssingle nucleotide variant
  • rs201927115Conflicting interpretationssingle nucleotide variant

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.