XRCC2 NM_005431.2(XRCC2):c.667T>C (p.Tyr223His)

CI-VAR-00020088Explore in graph →p.Tyr223HisNM_005431.2:c.667T>CClinVar 127962 rs587780130

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
127962	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome; Spermatogenic failure 50; Premature ovarian failure 17; Fanconi anemia complementation group U	germline	4	Apr 17, 2025	clinvar