PMM2 NM_000303.3(PMM2):c.447+5G>A

CI-VAR-00067817Explore in graph →NM_000303.3:c.447+5G>AClinVar 418663 rs367852554

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
418663	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	PMM2-congenital disorder of glycosylation; Ovarian serous cystadenocarcinoma	germline	5	Feb 16, 2026	clinvar