List of variants in gene combination ATP1A2, LOC126805890 reported as uncertain significance for Migraine, familial hemiplegic, 2

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000702.4(ATP1A2):c.627T>C (p.Cys209=)	rs139229302	0.00005
NM_000702.4(ATP1A2):c.736A>G (p.Asn246Asp)	rs764917849	0.00002
NM_000702.4(ATP1A2):c.631-6C>T	rs886045416
NM_000702.4(ATP1A2):c.671C>T (p.Thr224Ile)	rs1230517801

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