Variant · Snv
GM2A NM_000405.5(GM2A):c.*724G>C
CI-VAR-00155091Explore in graph →NM_000405.5:c.*724G>CClinVar 906601 rs112641014
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
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 906601 | Uncertain significance | criteria provided, multiple submitters, no conflicts | 2 | Tay-Sachs disease, variant AB; Uterine corpus endometrial carcinoma; Familial pancreatic carcinoma; Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Ovarian cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Lymphoma | germline | 3 | Jan 13, 2018 | clinvar |