HFE NM_000410.4(HFE):c.845G>A (p.Cys282Tyr)

CI-VAR-00005098Explore in graph →p.Cys282TyrNM_000410.4:c.845G>AClinVar 9 rs1800562

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
9	Pathogenic/Pathogenic, low penetrance; risk factor	criteria provided, multiple submitters, no conflicts	2	Hemochromatosis type 1; Hereditary cancer-predisposing syndrome; Hereditary hemochromatosis; Cutaneous photosensitivity; Porphyrinuria; Bronze diabetes; Cardiomyopathy; HFE-related disorder; Inborn genetic diseases; Juvenile hemochromatosis; Neuroendocrine neoplasm	germline	57	Aug 31, 2026	clinvar