Variant · Snv
NPHP4 NM_015102.5(NPHP4):c.518-2A>G
CI-VAR-00202590Explore in graph →NM_015102.5:c.518-2A>GClinVar 1324817 rs761142233
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 |
|---|---|---|---|---|---|---|---|---|
| 1324817 | Likely pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Nephronophthisis; Senior-Loken syndrome 4; Nephronophthisis 4; Clear cell carcinoma of kidney; Chronic lymphocytic leukemia/small lymphocytic lymphoma | germline | 4 | Jun 17, 2024 | clinvar |