List of variants in gene WWOX reported as benign by PreventionGenetics, part of Exact Sciences

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_016373.4(WWOX):c.516+6T>C	rs2303191	0.75307
NM_016373.4(WWOX):c.517-108260C>A	rs8050128	0.46958
NM_016373.4(WWOX):c.108-12G>T	rs67493355	0.34450
NM_016373.4(WWOX):c.-5C>T	rs11545028	0.27934
NM_016373.4(WWOX):c.606-17G>A	rs4130513	0.24208
NM_016373.4(WWOX):c.844C>G (p.Pro282Ala)	rs3764340	0.07330
NM_016373.4(WWOX):c.646C>G (p.Leu216Val)	rs7201683	0.03724
NM_016373.4(WWOX):c.941G>A (p.Arg314His)	rs73572838	0.03269
NM_016373.4(WWOX):c.547G>A (p.Asp183Asn)	rs74944733	0.02435
NM_016373.4(WWOX):c.293C>T (p.Pro98Leu)	rs144601717	0.01477
NM_016373.4(WWOX):c.613C>A (p.His205Asn)	rs74860463	0.00674
NM_016373.4(WWOX):c.468G>T (p.Arg156Ser)	rs140817689	0.00063
NM_016373.4(WWOX):c.409+16A>C	rs12934985
NM_016373.4(WWOX):c.535G>A (p.Ala179Thr)	rs11545029

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