Variant · Snv
PLA2G6 NM_003560.4(PLA2G6):c.1743-2A>G
CI-VAR-00298899Explore in graph →NM_003560.4:c.1743-2A>GClinVar 2501145 rs2087184707
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 |
|---|---|---|---|---|---|---|---|---|
| 2501145 | Pathogenic/Likely pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Neurodegeneration with brain iron accumulation; Infantile neuroaxonal dystrophy; Autosomal recessive Parkinson disease 14; Neurodegeneration with brain iron accumulation 2B; Papillary renal cell carcinoma type 1 | germline | 4 | Jun 11, 2024 | clinvar |