ATP1A2 NM_000702.4(ATP1A2):c.13-11_13-8del

CI-VAR-00025863Explore in graph →NM_000702.4:c.13-11_13-8delClinVar 166705 rs373796693

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
166705	Benign	criteria provided, multiple submitters, no conflicts	2	Familial hemiplegic migraine; Alternating hemiplegia of childhood 1; Migraine, familial hemiplegic, 2; Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies; Developmental and epileptic encephalopathy 98; Gastric cancer	germline	8	Feb 04, 2026	clinvar