List of variants in gene WWOX reported as pathogenic by GeneDx

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_016373.4(WWOX):c.790C>T (p.Arg264Ter)	rs756762196	0.00002
NM_016373.4(WWOX):c.131G>A (p.Trp44Ter)	rs1057517846
NM_016373.4(WWOX):c.132G>A (p.Trp44Ter)	rs1555535072
NM_016373.4(WWOX):c.255C>G (p.Tyr85Ter)	rs990150249
NM_016373.4(WWOX):c.410-1G>A	rs886039653
NM_016373.4(WWOX):c.606-1G>A	rs730882215
NM_016373.4(WWOX):c.689A>C (p.Gln230Pro)

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