List of variants in gene combination LOC102724058, SCN1A reported as benign for Severe myoclonic epilepsy in infancy

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Gene type: Distinguish antisense genes from sense genes
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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.3723T>C (p.Tyr1241=)	rs36031496	0.03789
NM_001165963.4(SCN1A):c.3521C>G (p.Thr1174Ser)	rs121918799	0.00159
NM_001165963.4(SCN1A):c.5782C>G (p.Arg1928Gly)	rs121917956	0.00073
NM_001165963.4(SCN1A):c.3924A>T (p.Glu1308Asp)	rs121917910	0.00070
NM_001165963.4(SCN1A):c.3749C>T (p.Thr1250Met)	rs140731963	0.00025
NM_001165963.4(SCN1A):c.4556C>T (p.Pro1519Leu)	rs372425457	0.00004
NM_001165963.4(SCN1A):c.4723C>T (p.Arg1575Cys)	rs121918807	0.00003
NM_001165963.4(SCN1A):c.4855A>G (p.Met1619Val)	rs373967247	0.00001

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