ClinVar Miner

List of variants in gene WWOX reported as likely pathogenic for Developmental and epileptic encephalopathy, 1

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.173-6T>G	rs200812468	0.00004
NM_016373.4(WWOX):c.136C>T (p.His46Tyr)	rs1597207871

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