FANCD2 NM_033084.6(FANCD2):c.2609_2613del

CI-VAR-00307798Explore in graph →NM_033084.6:c.2609_2613delClinVar 2675489 rs2469993551

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
2675489	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Fanconi anemia complementation group D2; Fanconi anemia	germline	2	Nov 14, 2023	clinvar