List of variants in gene WWOX reported as pathogenic for not provided

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: 21

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HGVS	dbSNP	gnomAD frequency
NM_016373.4(WWOX):c.749C>G (p.Ser250Ter)	rs368928190	0.00006
NM_016373.4(WWOX):c.790C>T (p.Arg264Ter)	rs756762196	0.00002
GRCh37/hg19 16q23.1(chr16:78128313-78151480)x1
GRCh37/hg19 16q23.1(chr16:78186513-78257627)x1
GRCh37/hg19 16q23.1(chr16:78272827-78367613)x1
GRCh37/hg19 16q23.1(chr16:78308767-78371608)x1
GRCh37/hg19 16q23.1(chr16:78374562-78469453)x1
GRCh37/hg19 16q23.1(chr16:78384724-78504169)x1
GRCh37/hg19 16q23.1(chr16:78402398-78504169)x1
GRCh37/hg19 16q23.1(chr16:78413243-78439784)x1
GRCh37/hg19 16q23.1(chr16:78420757-78466649)x1
GRCh37/hg19 16q23.1-23.2(chr16:79172680-79271549)x1
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.553_566del (p.Ala185fs)
NM_016373.4(WWOX):c.606-1G>A	rs730882215
NM_016373.4(WWOX):c.689A>C (p.Gln230Pro)
NM_016373.4(WWOX):c.716T>G (p.Leu239Arg)	rs2083042603
NM_016373.4(WWOX):c.854del (p.Asn285fs)	rs1394607357

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