CFH NM_000186.4(CFH):c.245-7G>A

CI-VAR-00050152Explore in graph →NM_000186.4:c.245-7G>AClinVar 294480 rs35814900

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
294480	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II; Hemolytic uremic syndrome, atypical, susceptibility to, 1; Basal laminar drusen; Age related macular degeneration 4; Atypical hemolytic-uremic syndrome; Factor H deficiency; Uterine carcinosarcoma; Thymoma; Cholangiocarcinoma; Acute myeloid leukemia; Gastric cancer; Lung cancer	germline	13	Apr 01, 2026	clinvar