ClinVar Miner

List of variants in gene SCN2A reported as likely pathogenic by Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001040142.2(SCN2A):c.1136G>A (p.Arg379His)	rs2105255398
NM_001040142.2(SCN2A):c.4904G>A (p.Arg1635Gln)	rs1057520844

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