IFNGR1 NM_000416.3(IFNGR1):c.*41G>A

CI-VAR-00155108Explore in graph →NM_000416.3:c.*41G>AClinVar 907652 rs17181562

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
907652	Benign	criteria provided, single submitter	1	Immunodeficiency 27A; Thyroid cancer, nonmedullary, 1; Nonpapillary renal cell carcinoma; Cervical cancer; Malignant tumor of esophagus	germline	2	Jan 13, 2018	clinvar