ClinVar Miner

List of variants in gene WWOX reported as benign for not specified

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Gene type:
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Total variants: 20
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HGVS dbSNP
NM_016373.3(WWOX):c.-5C>T rs11545028
NM_016373.3(WWOX):c.108-12G>T rs67493355
NM_016373.3(WWOX):c.108-12delG rs149533117
NM_016373.3(WWOX):c.293C>T (p.Pro98Leu) rs144601717
NM_016373.3(WWOX):c.351C>G (p.Leu117=) rs34944716
NM_016373.3(WWOX):c.358C>T (p.Arg120Trp) rs141361080
NM_016373.3(WWOX):c.409+16A>C rs12934985
NM_016373.3(WWOX):c.516+6T>C rs2303191
NM_016373.3(WWOX):c.535G>A (p.Ala179Thr) rs11545029
NM_016373.3(WWOX):c.547G>A (p.Asp183Asn) rs74944733
NM_016373.3(WWOX):c.606-17G>A rs4130513
NM_016373.3(WWOX):c.613C>A (p.His205Asn) rs74860463
NM_016373.3(WWOX):c.646C>G (p.Leu216Val) rs7201683
NM_016373.3(WWOX):c.754C>G (p.Pro252Ala) rs75559202
NM_016373.3(WWOX):c.835C>T (p.Arg279Cys) rs77314072
NM_016373.3(WWOX):c.844C>G (p.Pro282Ala) rs3764340
NM_016373.3(WWOX):c.876T>C (p.Ala292=) rs74030232
NM_016373.3(WWOX):c.885G>A (p.Arg295=) rs79771882
NM_016373.3(WWOX):c.888C>G (p.Ser296=) rs3764341
NM_016373.3(WWOX):c.941G>A (p.Arg314His) rs73572838

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