List of variants in gene ATP1A2 reported as uncertain significance for Alternating hemiplegia of childhood

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000702.4(ATP1A2):c.*1630C>T	rs886045433	0.00001
NM_000702.4(ATP1A2):c.*1241del	rs886045426
NM_000702.4(ATP1A2):c.*1333dup	rs538086614
NM_000702.4(ATP1A2):c.*1482del	rs886045430
NM_000702.4(ATP1A2):c.1547_1548delinsTT	rs886045432
NM_000702.4(ATP1A2):c.1643_1646del	rs533473532

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