COL4A2 NM_001846.4(COL4A2):c.2048G>C (p.Gly683Ala)

CI-VAR-00052943Explore in graph →p.Gly683AlaNM_001846.4:c.2048G>CClinVar 311143 rs3803230

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
311143	Benign	criteria provided, multiple submitters, no conflicts	2	Brain small vessel disease 2A, autosomal dominant; Malignant lymphoma, large B-cell, diffuse; Uterine carcinosarcoma; Colorectal cancer; Adrenocortical carcinoma, hereditary	germline	9	Feb 03, 2026	clinvar