GRIA3 NM_007325.5(GRIA3):c.1501-8T>A

CI-VAR-00020396Explore in graph →NM_007325.5:c.1501-8T>AClinVar 129168 rs139058646

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
129168	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Syndromic X-linked intellectual disability 94; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Ovarian serous cystadenocarcinoma	germline	12	Feb 03, 2026	clinvar