List of variants in gene combination LOC102724058, SCN1A reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.4547C>T (p.Ser1516Leu)	rs139300715	0.00003
NM_001165963.4(SCN1A):c.3391G>A (p.Asp1131Asn)	rs372555722	0.00001
NM_001165963.4(SCN1A):c.4342G>C (p.Glu1448Gln)	rs1193847815	0.00001
NM_001165963.4(SCN1A):c.4495T>C (p.Phe1499Leu)	rs121918632	0.00001
NM_001165963.4(SCN1A):c.4002+1G>T	rs1692153643
NM_001165963.4(SCN1A):c.4002+2322A>G
NM_001165963.4(SCN1A):c.4300T>A (p.Trp1434Arg)	rs121918789
NM_001165963.4(SCN1A):c.5139C>G (p.Ser1713Arg)
NM_001165963.4(SCN1A):c.5515C>G (p.Leu1839Val)	rs794726801
NM_001165963.4(SCN1A):c.5656C>T (p.Arg1886Ter)	rs779614747
NM_001165963.4(SCN1A):c.5782C>T (p.Arg1928Cys)	rs121917956

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