Variant · Snv
ALMS1 NM_001378454.1(ALMS1):c.11266G>A (p.Gly3756Ser)
CI-VAR-00034957Explore in graph →p.Gly3756SerNM_001378454.1:c.11266G>AClinVar 220878 rs34927702
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 |
|---|---|---|---|---|---|---|---|---|
| 220878 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Monogenic diabetes; Alstrom syndrome; Cardiovascular phenotype; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Sarcoma; Uterine carcinosarcoma; Thymoma; Nonpapillary renal cell carcinoma; Hepatocellular carcinoma; Cervical cancer | germline | 15 | Feb 03, 2026 | clinvar |