Gene entry

ARHGAP9

Rho GTPase activating protein 9

Chromosome: 12
Cytoband: 12q13.3
Variants (rsID): 8

ARHGAP9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q13.3). Its official name is “Rho GTPase activating protein 9”. The reference table lists 8 variants (rsID) for this gene.

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Clinically classified variants

2 reference-table entries with clinical significance.

rs11544238Uncertain significancesingle nucleotide variantCoronary artery spasm 3, susceptibility to
rs2277315Not classifiedmissense_variant

Other listed variants

rs34133632
rs61758883
rs73121618
rs79948748
rs147623082
rs190021861

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.