POMGNT1 NM_017739.4(POMGNT1):c.652+1G>A

CI-VAR-00005392Explore in graph →NM_017739.4:c.652+1G>AClinVar 3999 rs386834035

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
3999	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3; Muscle eye brain disease; Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3; Muscular dystrophy-dystroglycanopathy; Ovarian serous cystadenocarcinoma	germline	6	Jun 17, 2023	clinvar