List of variants in gene WWOX reported as uncertain significance by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_016373.4(WWOX):c.16T>C (p.Tyr6His)	rs1239497096
NM_016373.4(WWOX):c.517C>T (p.His173Tyr)	rs777272586
NM_016373.4(WWOX):c.791+18A>T	rs1023123497

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