POR NM_001395413.1(POR):c.1058-13C>G

CI-VAR-00022509Explore in graph →NM_001395413.1:c.1058-13C>GClinVar 138789 rs4732516

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
138789	Benign	criteria provided, multiple submitters, no conflicts	2	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency; 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia; Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis; Hepatocellular carcinoma	germline	12	Feb 04, 2026	clinvar