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

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.1178G>A (p.Arg393His)	rs121917927
NM_001165963.4(SCN1A):c.1922_1923delinsATC (p.Met641fs)	rs1697433995
NM_001165963.4(SCN1A):c.264+5G>A	rs794726762
NM_001165963.4(SCN1A):c.2732T>G (p.Leu911Arg)
NM_001165963.4(SCN1A):c.602+3_602+6del	rs1698937795
NM_001165963.4(SCN1A):c.680T>C (p.Ile227Thr)	rs121917937
NM_001165963.4(SCN1A):c.941G>A (p.Trp314Ter)	rs1698574524

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