Variant · Snv
PHGDH NM_006623.4(PHGDH):c.792+6T>G
CI-VAR-00071738Explore in graph →NM_006623.4:c.792+6T>GClinVar 447938 rs146953046
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 |
|---|---|---|---|---|---|---|---|---|
| 447938 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | PHGDH deficiency; Neu-Laxova syndrome 1; Uveal melanoma; Gastric cancer; Malignant tumor of esophagus; Lung cancer; Uterine corpus endometrial carcinoma; Familial cancer of breast; Ovarian cancer; Sarcoma; Lymphoma; Nonpapillary renal cell carcinoma; Cervical cancer; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Thymoma; Cholangiocarcinoma; Acute myeloid leukemia | germline | 11 | Mar 01, 2026 | clinvar |