ClinVar Miner

List of variants reported as likely pathogenic by VIB - Center for Molecular Neurology, University of Antwerp

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.265-2143G>A	rs1574312497
NM_001165963.4(SCN1A):c.4338+616G>A	rs1366966423

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