List of variants in gene SCN1A reported as pathogenic for Migraine, familial hemiplegic, 3

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.1028+2T>C	rs1698170849
NM_001165963.4(SCN1A):c.1178G>A (p.Arg393His)	rs121917927
NM_001165963.4(SCN1A):c.1702C>T (p.Arg568Ter)	rs886039430
NM_001165963.4(SCN1A):c.1843G>T (p.Gly615Ter)	rs1271824691
NM_001165963.4(SCN1A):c.2792G>A (p.Arg931His)	rs794726718
NM_001165963.4(SCN1A):c.2854T>A (p.Trp952Arg)
NM_001165963.4(SCN1A):c.2946+2T>C
NM_001165963.4(SCN1A):c.301C>T (p.Arg101Trp)	rs121917965
NM_001165963.4(SCN1A):c.302G>A (p.Arg101Gln)	rs121917918
NM_001165963.4(SCN1A):c.602+1G>A
NM_001165963.4(SCN1A):c.659T>A (p.Val220Asp)
NM_001165963.4(SCN1A):c.828A>C (p.Lys276Asn)

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