List of variants in gene SCN1A reported as likely benign for Familial hemiplegic migraine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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.1171-10_1171-9del	rs372840031
NM_001165963.4(SCN1A):c.2044-5del	rs549232924
NM_001165963.4(SCN1A):c.2177-8dup	rs747086735

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