List of variants reported as uncertain significance for Migraine, familial hemiplegic, 2 by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000702.4(ATP1A2):c.736A>G (p.Asn246Asp)	rs764917849	0.00002
NM_000702.4(ATP1A2):c.1465T>C (p.Ser489Pro)
NM_000702.4(ATP1A2):c.2450T>A (p.Ile817Asn)
NM_000702.4(ATP1A2):c.2620G>A (p.Gly874Ser)	rs1651959213

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