List of variants in gene SCN1A studied 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
		ClinVar version:

Total variants: 5

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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.2177-11dup	rs11394960
NM_001165963.4(SCN1A):c.2177-8dup	rs747086735
NM_001165963.4(SCN1A):c.787C>G (p.Leu263Val)	rs2105890052

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