RANBP2 NM_006267.5(RANBP2):c.7849+4A>G

CI-VAR-00056040Explore in graph →NM_006267.5:c.7849+4A>GClinVar 382464 rs2949961

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
382464	Benign	criteria provided, multiple submitters, no conflicts	2	Familial acute necrotizing encephalopathy; Familial pancreatic carcinoma; Ovarian serous cystadenocarcinoma; Hepatocellular carcinoma; Malignant tumor of esophagus; Familial cancer of breast; Nonpapillary renal cell carcinoma	germline	5	Jan 15, 2026	clinvar