List of variants in gene WWOX reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_016373.4(WWOX):c.885G>A (p.Arg295=)	rs79771882	0.00946
NM_016373.4(WWOX):c.613C>A (p.His205Asn)	rs74860463	0.00674
NM_016373.4(WWOX):c.358C>T (p.Arg120Trp)	rs141361080	0.00523
NM_016373.4(WWOX):c.816G>T (p.Leu272Phe)	rs186745328	0.00280
NM_016373.4(WWOX):c.605+9T>A	rs368853054	0.00069
NM_016373.4(WWOX):c.807C>T (p.Asn269=)	rs62034095	0.00067
NM_016373.4(WWOX):c.552C>T (p.Leu184=)	rs199715254	0.00029
NM_016373.4(WWOX):c.898A>G (p.Asn300Asp)	rs374541202	0.00012
NM_016373.4(WWOX):c.635C>T (p.Ala212Val)	rs202006159	0.00008
NM_016373.4(WWOX):c.114C>T (p.Thr38=)	rs372635270	0.00004
NM_016373.4(WWOX):c.605T>G (p.Val202Gly)	rs112636835	0.00004
NM_016373.4(WWOX):c.919C>G (p.Leu307Val)	rs200320711	0.00002
NM_016373.4(WWOX):c.948C>G (p.Val316=)	rs201986739	0.00001
NM_016373.4(WWOX):c.608C>G (p.Pro203Arg)	rs1405481740
NM_016373.4(WWOX):c.656G>C (p.Ser219Thr)	rs367599412
NM_016373.4(WWOX):c.876T>G (p.Ala292=)	rs74030232
NM_016373.4(WWOX):c.935C>T (p.Ser312Phe)	rs79399971

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