List of variants reported as uncertain significance for Familial hemiplegic migraine by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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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
NM_000702.4(ATP1A2):c.528G>T (p.Met176Ile)	rs867416764
NM_001165963.4(SCN1A):c.*1872del	rs878898132
NM_001165963.4(SCN1A):c.672_675del	rs886055038
NM_001165963.4(SCN1A):c.*878dup	rs886055037

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