ClinVar Miner

List of variants in gene WWOX reported as pathogenic for childhood epilepsy with centrotemporal spikes

Included ClinVar conditions (3):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_016373.4(WWOX):c.754C>G (p.Pro252Ala)	rs75559202	0.00684
NM_016373.4(WWOX):c.990C>G (p.Asn330Lys)	rs117209694	0.00016

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