ClinVar Miner

List of variants in gene SCN8A reported as pathogenic by GeneReviews

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: 1

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HGVS	dbSNP	gnomAD frequency
NP_055006.1(SCN8A):p.Pro1428_Lys1473del

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