RIPOR2 NM_001286445.3(RIPOR2):c.1164+482A>G

CI-VAR-00239747Explore in graph →NM_001286445.3:c.1164+482A>GClinVar 1680505 rs745360194

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
1680505	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Autosomal dominant nonsyndromic hearing loss 21; Autosomal recessive nonsyndromic hearing loss 104; Chronic lymphocytic leukemia/small lymphocytic lymphoma	germline	5	Oct 31, 2025	clinvar