List of variants in gene combination LOC102724058, SCN1A reported as uncertain significance for Familial hemiplegic migraine

Minimum submission review status:		Collection method:
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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: 3

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HGVS	dbSNP	gnomAD frequency
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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