List of variants in gene combination LOC102724058, SCN1A reported as benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.3705+33T>G	rs76743139	0.00915
NM_001165963.4(SCN1A):c.5864T>C (p.Ile1955Thr)	rs35735053	0.00876
NM_001165963.4(SCN1A):c.*677G>A	rs142037381	0.00168
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	0.00065
NM_001165963.4(SCN1A):c.4872G>A (p.Leu1624=)	rs142910512	0.00048
NM_001165963.4(SCN1A):c.5286A>G (p.Gly1762=)	rs150570058	0.00040
NM_001165963.4(SCN1A):c.4855A>G (p.Met1619Val)	rs373967247	0.00001
NM_001165963.4(SCN1A):c.*1872del	rs878898132

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