List of variants in gene SCN8A reported as benign by PreventionGenetics, part of Exact Sciences

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: 8

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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.3490+20G>A	rs303808	0.76481
NM_001330260.2(SCN8A):c.4509T>C (p.Pro1503=)	rs303815	0.62374
NM_001330260.2(SCN8A):c.4281+13A>G	rs9943809	0.08096
NM_001330260.2(SCN8A):c.3076C>T (p.Arg1026Cys)	rs117217073	0.01112
NM_001330260.2(SCN8A):c.2632C>T (p.Leu878=)	rs372582842	0.00185
NM_001330260.2(SCN8A):c.2131+7G>T	rs756286753
NM_001330260.2(SCN8A):c.5472C>A (p.Pro1824=)	rs60637

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