VWF NM_000552.5(VWF):c.3797C>A (p.Pro1266Gln)

CI-VAR-00018531Explore in graph →p.Pro1266GlnNM_000552.5:c.3797C>AClinVar 100279 rs61749370

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
100279	Uncertain significance	reviewed by expert panel	3	Hereditary von Willebrand disease; von Willebrand disease type 2; von Willebrand disease type 1; von Willebrand disease type 3; EBV-positive nodal T- and NK-cell lymphoma; VWF-related disorder	germline	21	May 06, 2025	clinvar