FOXP1 NM_001349338.3(FOXP1):c.1722+5G>C

CI-VAR-00325634Explore in graph →NM_001349338.3:c.1722+5G>CClinVar 2842204 rs2545010995

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
2842204	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Intellectual disability-severe speech delay-mild dysmorphism syndrome; Familial cancer of breast	germline	3	Mar 03, 2023	clinvar