List of variants in gene combination LOC102724058, SCN1A reported as likely benign by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.4731T>C (p.Asn1577=)	rs145296488	0.00114
NM_001165963.4(SCN1A):c.3101T>C (p.Ile1034Thr)	rs121918818	0.00084
NM_001165963.4(SCN1A):c.3948G>A (p.Arg1316=)	rs149579028	0.00073
NM_001165963.4(SCN1A):c.5782C>G (p.Arg1928Gly)	rs121917956	0.00073
NM_001165963.4(SCN1A):c.5286A>G (p.Gly1762=)	rs150570058	0.00040
NM_001165963.4(SCN1A):c.3450C>T (p.Ser1150=)	rs727504137	0.00002

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