FGA NM_021871.4(FGA):c.99C>T (p.Gly33=)

CI-VAR-00362972Explore in graph →p.Gly33=NM_021871.4:c.99C>TClinVar 3590356

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
3590356	Uncertain significance	criteria provided, single submitter	1	Familial dysfibrinogenemia; Congenital afibrinogenemia; Familial visceral amyloidosis, Ostertag type; Uterine corpus endometrial carcinoma	germline	2	Apr 17, 2024	clinvar