Variant · Snv
GLRB NM_000824.5(GLRB):c.904+4A>T
CI-VAR-00050827Explore in graph →NM_000824.5:c.904+4A>TClinVar 347923 rs76714257
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
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 347923 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Hyperekplexia 2; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Lung cancer; Cervical cancer; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Colon adenocarcinoma; Colorectal cancer; Thymoma | germline | 6 | Feb 03, 2026 | clinvar |