ClinVar Miner

List of variants reported as pathogenic for Migraine, familial hemiplegic, 2 by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000702.4(ATP1A2):c.1643G>A (p.Arg548His)	rs121918616
NM_000702.4(ATP1A2):c.2936C>T (p.Pro979Leu)	rs121918615
NM_000702.4(ATP1A2):c.3005G>A (p.Arg1002Gln)	rs757310141

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