ARHGAP18 NM_033515.3(ARHGAP18):c.94G>A (p.Gly32Arg)

CI-VAR-00127003Explore in graph →p.Gly32ArgNM_033515.3:c.94G>AClinVar 783473 rs34390841

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
783473	Benign	criteria provided, single submitter	1	Acute myeloid leukemia; Clear cell carcinoma of kidney; Gastric cancer; Uterine carcinosarcoma; Colorectal cancer; Ovarian serous cystadenocarcinoma	germline	2	Dec 31, 2019	clinvar