List of variants reported as likely benign for Migraine, familial hemiplegic, 2 by Illumina Laboratory Services, Illumina

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000702.4(ATP1A2):c.25T>A (p.Tyr9Asn)	rs55858252	0.00211
NM_000702.4(ATP1A2):c.340G>A (p.Gly114Ser)	rs116711766	0.00071
NM_000702.4(ATP1A2):c.2751G>A (p.Thr917=)	rs146839867	0.00069
NM_000702.4(ATP1A2):c.1474G>A (p.Glu492Lys)	rs142348542	0.00055
NM_000702.4(ATP1A2):c.339C>T (p.Tyr113=)	rs148929192	0.00023
NM_000702.4(ATP1A2):c.2130C>T (p.Ala710=)	rs374749325	0.00021
NM_000702.4(ATP1A2):c.1666A>T (p.Asn556Tyr)	rs141467566	0.00019
NM_000702.4(ATP1A2):c.1582G>A (p.Asp528Asn)	rs374501280	0.00009
NM_000702.4(ATP1A2):c.*15G>A	rs187737212	0.00007
NM_000702.4(ATP1A2):c.2142C>T (p.Asp714=)	rs139022921	0.00007
NM_000702.4(ATP1A2):c.969C>T (p.Ile323=)	rs28716941	0.00004
NM_000702.4(ATP1A2):c.151C>T (p.Arg51Cys)	rs747283283	0.00002
NM_000702.4(ATP1A2):c.1572G>A (p.Glu524=)	rs775192056	0.00002
NM_000702.4(ATP1A2):c.2412C>T (p.Ile804=)	rs143969080	0.00002
NM_000702.4(ATP1A2):c.*1000T>A	rs116194737
NM_000702.4(ATP1A2):c.1652-7C>A	rs200102433

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