List of variants reported as uncertain significance for Severe myoclonic epilepsy in infancy by Mendelics

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.3714A>C (p.Glu1238Asp)	rs121917973	0.00008
NM_001165963.4(SCN1A):c.2686G>A (p.Val896Ile)	rs745378416	0.00001
NM_001165963.4(SCN1A):c.1898C>T (p.Ala633Val)	rs1574215846
NM_001165963.4(SCN1A):c.2012T>C (p.Val671Ala)	rs1574214843
NM_001165963.4(SCN1A):c.2177-2A>T	rs1436792531
NM_001165963.4(SCN1A):c.404T>C (p.Met135Thr)	rs1574290850
NM_001165963.4(SCN1A):c.5681T>C (p.Met1894Thr)	rs562208324
NM_001165963.4(SCN1A):c.635T>C (p.Val212Ala)	rs551068385

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