ARHGEF9 NM_001353921.2(ARHGEF9):c.1322-49T>G

CI-VAR-00113458Explore in graph →NM_001353921.2:c.1322-49T>GClinVar 633480 rs56401522

Curated evidence

Evidence by cancer (0 items)

Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.

Data not yet available

No curated evidence item references this variant yet.

ClinVar

Clinical significance (1)

ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.

clinvarCurated1 interpretation · review status and star rating as assigned by ClinVar.

Variation	Clinical significance	Review status	Stars	Conditions	Origin	Submitters	Last evaluated	Source
633480	Benign	criteria provided, multiple submitters, no conflicts	2	Epilepsy; Uterine corpus endometrial carcinoma; Malignant tumor of esophagus; Cervical cancer; Sarcoma; Ovarian serous cystadenocarcinoma; Thymoma; Acute myeloid leukemia; Lung cancer; Familial cancer of breast	germline	4	Jun 28, 2018	clinvar