MMP20 NM_004771.4(MMP20):c.954-2A>T

CI-VAR-00005479Explore in graph →NM_004771.4:c.954-2A>TClinVar 5428 rs140213840

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
5428	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Amelogenesis imperfecta hypomaturation type 2A2; MMP20-related disorder; Inborn genetic diseases; Gastric cancer	germline	12	Jan 20, 2026	clinvar