FBXO38 NM_205836.3(FBXO38):c.593-13A>T

CI-VAR-00199123Explore in graph →NM_205836.3:c.593-13A>TClinVar 1234143 rs61555444

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
1234143	Benign	criteria provided, multiple submitters, no conflicts	2	Distal hereditary motor neuropathy type 2; Acute myeloid leukemia; Malignant tumor of esophagus; Gastric cancer	germline	3	Jan 22, 2026	clinvar