ClinVar Miner

List of variants in gene WWOX reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_016373.4(WWOX):c.516+6T>C rs2303191 0.75307
NM_016373.4(WWOX):c.1056+191744T>G rs2548861 0.51877
NM_016373.4(WWOX):c.517-108260C>A rs8050128 0.46958
NM_016373.4(WWOX):c.409+122A>C rs7203387 0.40944
NM_016373.4(WWOX):c.173-68C>T rs2287972 0.40799
NM_016373.4(WWOX):c.108-12G>T rs67493355 0.34450
NM_016373.4(WWOX):c.-5C>T rs11545028 0.27934
NM_016373.4(WWOX):c.791+203G>C rs4129722 0.26952
NM_016373.4(WWOX):c.410-169T>C rs4359451 0.26780
NM_016373.4(WWOX):c.606-17G>A rs4130513 0.24208
NM_016373.4(WWOX):c.1056+109A>C rs3764342 0.22979
NM_016373.4(WWOX):c.231-43C>T rs12934051 0.22349
NM_016373.4(WWOX):c.516+50G>A rs2303190 0.13252
NM_016373.4(WWOX):c.410-296A>T rs62045116 0.13247
NM_016373.4(WWOX):c.410-249G>A rs62045118 0.13025
NM_016373.4(WWOX):c.516+316T>C rs12325408 0.12626
NM_016373.4(WWOX):c.606-150G>A rs6564553 0.08926
NM_016373.4(WWOX):c.517-108268G>T rs8048830 0.08859
NM_016373.4(WWOX):c.605+138G>A rs61054844 0.08638
NM_016373.4(WWOX):c.844C>G (p.Pro282Ala) rs3764340 0.07330
NM_016373.4(WWOX):c.517-296A>G rs72796085 0.07170
NM_016373.4(WWOX):c.517-115G>A rs35121047 0.06434
NM_016373.4(WWOX):c.605+37C>T rs12446823 0.06010
NM_016373.4(WWOX):c.517-108230A>G rs77067228 0.05744
NM_016373.4(WWOX):c.606-183G>A rs67266598 0.04985
NC_000016.10:g.78099226T>C rs77018334 0.04939
NM_016373.4(WWOX):c.791+68C>G rs7202218 0.04867
NM_016373.4(WWOX):c.606-68G>A rs74618473 0.04840
NM_016373.4(WWOX):c.231-129T>A rs2072587 0.04660
NM_016373.4(WWOX):c.231-233G>A rs7200257 0.04607
NM_016373.4(WWOX):c.646C>G (p.Leu216Val) rs7201683 0.03724
NM_016373.4(WWOX):c.941G>A (p.Arg314His) rs73572838 0.03269
NM_016373.4(WWOX):c.791+228T>A rs78891306 0.03197
NM_016373.4(WWOX):c.547G>A (p.Asp183Asn) rs74944733 0.02435
NM_016373.4(WWOX):c.172+103C>G rs73562780 0.02172
NM_016373.4(WWOX):c.230+104C>T rs79221901 0.02138
NM_016373.4(WWOX):c.410-56A>T rs114757033 0.01855
NM_016373.4(WWOX):c.108-171C>G rs73562775 0.01805
NM_016373.4(WWOX):c.108-12del rs149533117 0.01497
NM_016373.4(WWOX):c.108-76A>G rs79294211 0.01485
NM_016373.4(WWOX):c.293C>T (p.Pro98Leu) rs144601717 0.01477
NM_016373.4(WWOX):c.351C>G (p.Leu117=) rs34944716 0.01231
NM_016373.4(WWOX):c.885G>A (p.Arg295=) rs79771882 0.00946
NM_016373.4(WWOX):c.754C>G (p.Pro252Ala) rs75559202 0.00684
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.835C>T (p.Arg279Cys) rs77314072 0.00444
NM_016373.4(WWOX):c.888C>G (p.Ser296=) rs3764341 0.00102
NM_016373.4(WWOX):c.468G>T (p.Arg156Ser) rs140817689 0.00063
GRCh38/hg38 16q23.1(chr16:78624328-78711823)x1
NM_016373.4(WWOX):c.1056+269del rs58363153
NM_016373.4(WWOX):c.108-111T>C rs4887937
NM_016373.4(WWOX):c.108-13dup rs146697931
NM_016373.4(WWOX):c.231-79T>G rs1469117
NM_016373.4(WWOX):c.409+16A>C rs12934985
NM_016373.4(WWOX):c.410-270C>T rs62045117
NM_016373.4(WWOX):c.517-108020G>A rs76484313
NM_016373.4(WWOX):c.517-158C>G rs9932296
NM_016373.4(WWOX):c.517-177del rs61469070
NM_016373.4(WWOX):c.535G>A (p.Ala179Thr) rs11545029
NM_016373.4(WWOX):c.606-254C>T rs8059174
NM_016373.4(WWOX):c.606-283T>C rs8064007
NM_016373.4(WWOX):c.606-296G>C rs8057749
NM_016373.4(WWOX):c.606-303A>T rs79064575
NM_016373.4(WWOX):c.792-123C>G rs113764353
NM_016373.4(WWOX):c.792-154G>A rs11866497
NM_016373.4(WWOX):c.792-300G>C rs111619900
NM_016373.4(WWOX):c.876T>C (p.Ala292=) rs74030232

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