PBX1 NM_002585.4(PBX1):c.511-2A>G

CI-VAR-00070882Explore in graph →NM_002585.4:c.511-2A>GClinVar 437837 rs1553248075

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
437837	Pathogenic	no assertion criteria provided	0	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay; Familial pancreatic carcinoma	germline	2	Aug 25, 2017	clinvar