COL1A2 NM_000089.4(COL1A2):c.892-13C>G

CI-VAR-00051465Explore in graph →NM_000089.4:c.892-13C>GClinVar 360949 rs200532328

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
360949	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Osteogenesis imperfecta; Ehlers-Danlos syndrome, arthrochalasia type, 2; Osteogenesis imperfecta type I; Ehlers-Danlos syndrome, classic type, 1; Malignant tumor of esophagus	germline	7	Jun 29, 2026	clinvar