List of variants in gene SCN1A reported as not provided for genetic generalized epilepsy

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.80G>C (p.Arg27Thr)	rs121917906	0.00006
NM_001165963.4(SCN1A):c.1130G>A (p.Arg377Gln)	rs121917957
NM_001165963.4(SCN1A):c.1162T>C (p.Tyr388His)	rs121918781
NM_001165963.4(SCN1A):c.220T>C (p.Ser74Pro)	rs121917931
NM_001165963.4(SCN1A):c.2369A>G (p.Tyr790Cys)	rs121918782
NM_001165963.4(SCN1A):c.238dup (p.Leu80fs)	rs1684663586
NM_001165963.4(SCN1A):c.2575C>T (p.Arg859Cys)	rs121918784
NM_001165963.4(SCN1A):c.2624C>T (p.Thr875Met)	rs121918623
NM_001165963.4(SCN1A):c.345T>A (p.Asn115Lys)	rs61741123
NM_001165963.4(SCN1A):c.434T>C (p.Met145Thr)	rs121918631
NM_001165963.4(SCN1A):c.563A>T (p.Asp188Val)	rs121917953

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