ATP1A2 NM_000702.4(ATP1A2):c.1652-11C>G

CI-VAR-00046954Explore in graph →NM_000702.4:c.1652-11C>GClinVar 256763 rs17846713

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.

clinvarCurated1 interpretation · review status and star rating as assigned by ClinVar.

Variation	Clinical significance	Review status	Stars	Conditions	Origin	Submitters	Last evaluated	Source
256763	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Alternating hemiplegia of childhood 1; Migraine, familial hemiplegic, 2; Familial hemiplegic migraine; Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies; Developmental and epileptic encephalopathy 98; Gastric cancer; Thymoma; Lymphoma; Malignant tumor of esophagus; Uterine corpus endometrial carcinoma	germline	11	Feb 03, 2026	clinvar