Variant · Snv
IFIH1 NM_022168.4(IFIH1):c.2807+1G>A
CI-VAR-00094732Explore in graph →NM_022168.4:c.2807+1G>AClinVar 541779 rs35732034
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 |
|---|---|---|---|---|---|---|---|---|
| 541779 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Aicardi-Goutieres syndrome 7; Singleton-Merten syndrome 1; Immunodeficiency 95; IFIH1-related disorder; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Colon adenocarcinoma; Sarcoma; Acute myeloid leukemia; Malignant tumor of esophagus; Familial cancer of breast; Clear cell carcinoma of kidney; Uveal melanoma; Familial pancreatic carcinoma; Malignant lymphoma, large B-cell, diffuse; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Lung cancer; Cervical cancer; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Thymoma; Thyroid cancer, nonmedullary, 1; Uterine corpus endometrial carcinoma; Colorectal cancer; Gastric cancer; Melanoma; Hepatocellular carcinoma; Ovarian cancer | germline | 14 | Apr 23, 2026 | clinvar |