PGAP1 NM_024989.4(PGAP1):c.1862-3C>T

CI-VAR-00122678Explore in graph →NM_024989.4:c.1862-3C>TClinVar 673057 rs73988069

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
673057	Benign	criteria provided, multiple submitters, no conflicts	2	Intellectual disability, autosomal recessive 42; Hereditary spastic paraplegia; Thymoma; Cholangiocarcinoma; Acute myeloid leukemia; Malignant tumor of esophagus; Ovarian serous cystadenocarcinoma; Nonpapillary renal cell carcinoma; Lung cancer; Familial cancer of breast; Adrenocortical carcinoma, hereditary; Cervical cancer	germline	6	Feb 01, 2026	clinvar