Variant · Snv
HSPG2 NM_005529.7(HSPG2):c.7806C>A (p.Val2602=)
CI-VAR-00050141Explore in graph →p.Val2602=NM_005529.7:c.7806C>AClinVar 295785 rs12737091
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.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 295785 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Lethal Kniest-like syndrome; Schwartz-Jampel syndrome; Connective tissue disorder; Colon adenocarcinoma; Colorectal cancer; Lymphoma; Uterine carcinosarcoma; Thymoma; Adrenocortical carcinoma, hereditary; Ovarian cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Familial pancreatic carcinoma; Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Uterine corpus endometrial carcinoma; Uveal melanoma; Cholangiocarcinoma; Hepatocellular carcinoma | germline | 8 | Feb 04, 2026 | clinvar |