RANBP2 NM_006267.5(RANBP2):c.73-6T>A

CI-VAR-00071699Explore in graph →NM_006267.5:c.73-6T>AClinVar 446012 rs201485597

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
446012	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Familial acute necrotizing encephalopathy; Uterine corpus endometrial carcinoma; Ovarian serous cystadenocarcinoma; Thymoma; Acute myeloid leukemia; Lung cancer; Malignant tumor of esophagus; Familial cancer of breast	germline	8	Jun 01, 2026	clinvar