Variant · Snv
HCN2 NM_001194.4(HCN2):c.1584+7C>T
CI-VAR-00058679Explore in graph →NM_001194.4:c.1584+7C>TClinVar 402923 rs55978915
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
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 402923 | Likely benign | criteria provided, single submitter | 1 | HCN2-related disorder; Lung cancer; Cervical cancer; Thymoma; Malignant tumor of esophagus; Uveal melanoma; Sarcoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Uterine corpus endometrial carcinoma; Uterine carcinosarcoma; Acute myeloid leukemia | germline | 3 | Apr 25, 2016 | clinvar |