List of variants in gene SCN8A reported as 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001330260.2(SCN8A):c.576C>T (p.Asp192=)	rs4761829	0.81114
NM_001330260.2(SCN8A):c.1833G>T (p.Arg611=)	rs35242963	0.01438
NM_001330260.2(SCN8A):c.2632C>T (p.Leu878=)	rs372582842	0.00185
NM_001330260.2(SCN8A):c.4278G>A (p.Arg1426=)	rs143867796	0.00183
NM_001330260.2(SCN8A):c.2098A>T (p.Ile700Leu)	rs187153231	0.00138
NM_001330260.2(SCN8A):c.2371-6A>G	rs187002252	0.00061
NM_001330260.2(SCN8A):c.5472C>A (p.Pro1824=)	rs60637

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