ClinVar Miner

List of variants in gene WWOX reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 22
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HGVS dbSNP
NM_016373.4(WWOX):c.1019T>C (p.Leu340Pro) rs761125565
NM_016373.4(WWOX):c.1044C>A (p.Phe348Leu) rs1057524658
NM_016373.4(WWOX):c.251C>G (p.Thr84Ser) rs757145186
NM_016373.4(WWOX):c.322G>A (p.Asp108Asn) rs747575799
NM_016373.4(WWOX):c.332C>G (p.Thr111Ser) rs114755364
NM_016373.4(WWOX):c.341T>C (p.Met114Thr) rs761906386
NM_016373.4(WWOX):c.421G>A (p.Ala141Thr) rs369907002
NM_016373.4(WWOX):c.468G>T (p.Arg156Ser) rs140817689
NM_016373.4(WWOX):c.499C>T (p.Arg167Cys) rs201228765
NM_016373.4(WWOX):c.524C>T (p.Ala175Val) rs1131691324
NM_016373.4(WWOX):c.566G>A (p.Ser189Asn) rs776354746
NM_016373.4(WWOX):c.591C>G (p.Phe197Leu) rs200847456
NM_016373.4(WWOX):c.673C>G (p.Leu225Val) rs376040091
NM_016373.4(WWOX):c.688C>G (p.Gln230Glu) rs1057524749
NM_016373.4(WWOX):c.713A>G (p.Tyr238Cys) rs142806268
NM_016373.4(WWOX):c.718G>T (p.Val240Phe) rs1057517847
NM_016373.4(WWOX):c.745C>A (p.Arg249Ser) rs749277249
NM_016373.4(WWOX):c.766A>T (p.Ile256Phe) rs1023419687
NM_016373.4(WWOX):c.767T>C (p.Ile256Thr) rs775895501
NM_016373.4(WWOX):c.851A>G (p.Lys284Arg) rs897453553
NM_016373.4(WWOX):c.856G>A (p.Asp286Asn) rs374658336
NM_016373.4(WWOX):c.856G>T (p.Asp286Tyr) rs374658336

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