COL11A2 NM_080680.3(COL11A2):c.2484+22C>G

CI-VAR-00047242Explore in graph →NM_080680.3:c.2484+22C>GClinVar 262309 rs2744512

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
262309	Benign	criteria provided, multiple submitters, no conflicts	2	Autosomal dominant nonsyndromic hearing loss 13; Fibrochondrogenesis 2; Otospondylomegaepiphyseal dysplasia, autosomal recessive; Autosomal recessive nonsyndromic hearing loss 53; Otospondylomegaepiphyseal dysplasia, autosomal dominant; Hepatocellular carcinoma; Familial cancer of breast	germline	4	Jul 22, 2021	clinvar