CYP21A2 NM_000500.9(CYP21A2):c.844G>T (p.Val282Leu)

CI-VAR-00006005Explore in graph →p.Val282LeuNM_000500.9:c.844G>TClinVar 12151 rs6471

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
12151	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Carcinoma, adrenocortical, androgen-secreting; 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia; Adenoma, cortisol-producing; Inborn genetic diseases; Congenital adrenal hyperplasia; CYP21A2-related disorder	germline	41	Jul 18, 2026	clinvar