BLM NM_000057.4(BLM):c.99-8_112del

CI-VAR-00211020Explore in graph →NM_000057.4:c.99-8_112delClinVar 1500163 rs2151146678

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
1500163	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Bloom syndrome; Hereditary cancer-predisposing syndrome; Colorectal cancer	germline	4	Jun 09, 2025	clinvar