Gene entry

ARHGEF9

Cdc42 guanine nucleotide exchange factor 9

Chromosome: X
Cytoband: Xq11.1
Variants (rsID): 7

ARHGEF9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq11.1). Its official name is “Cdc42 guanine nucleotide exchange factor 9”. The reference table lists 7 variants (rsID) for this gene.

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Clinically classified variants

2 reference-table entries with clinical significance.

rs55868891Benignsingle nucleotide variantDevelopmental and epileptic encephalopathy, 8
rs121918361Pathogenicsingle nucleotide variantDevelopmental and epileptic encephalopathy, 8

Other listed variants

rs5964688
rs12844754
rs145322060
rs367891687
rs782156826

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.