ClinVar Miner

List of variants in gene WRN reported by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 84
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HGVS dbSNP
NM_000553.4(WRN):c.*194C>T rs11574411
NM_000553.4(WRN):c.*458T>A rs886062895
NM_000553.4(WRN):c.*511C>T rs11574413
NM_000553.4(WRN):c.*543C>G rs11574414
NM_000553.4(WRN):c.*570A>G rs11574415
NM_000553.4(WRN):c.*588A>G rs777411815
NM_000553.4(WRN):c.*626A>G rs886062897
NM_000553.4(WRN):c.-152G>A rs886062885
NM_000553.4(WRN):c.-163C>G rs11574160
NM_000553.4(WRN):c.-197C>T rs11574159
NM_000553.4(WRN):c.-209T>G rs886062884
NM_000553.4(WRN):c.-213G>A rs11574158
NM_000553.4(WRN):c.-234T>A rs886062883
NM_000553.4(WRN):c.-240G>A rs867674808
NM_000553.4(WRN):c.-278G>C rs11574157
NM_000553.4(WRN):c.-289delG rs886062880
NM_000553.4(WRN):c.-295_-294insG rs886062879
NM_000553.4(WRN):c.-380G>A rs886062877
NM_000553.4(WRN):c.-408C>T rs11574156
NM_000553.4(WRN):c.-437C>T rs886062876
NM_000553.4(WRN):c.-519C>A rs545194854
NM_000553.4(WRN):c.-605C>A rs11574155
NM_000553.4(WRN):c.-618C>G rs7017069
NM_000553.4(WRN):c.-636G>C rs886062875
NM_000553.4(WRN):c.-677G>T rs886062874
NM_000553.4(WRN):c.-683G>T rs886062873
NM_000553.4(WRN):c.106C>T (p.Arg36Trp) rs141495269
NM_000553.4(WRN):c.1466C>T (p.Pro489Leu) rs750052448
NM_000553.4(WRN):c.1530A>T (p.Glu510Asp) rs149565907
NM_000553.4(WRN):c.1577-3C>A rs3087409
NM_000553.4(WRN):c.1717A>G (p.Thr573Ala) rs150148567
NM_000553.4(WRN):c.1795A>G (p.Ile599Val) rs368931681
NM_000553.4(WRN):c.1831A>G (p.Met611Val) rs762866297
NM_000553.4(WRN):c.1981+11A>G rs189999761
NM_000553.4(WRN):c.1982-5delT rs397723919
NM_000553.4(WRN):c.2088+6C>T rs886062888
NM_000553.4(WRN):c.2128A>G (p.Ile710Val) rs180814740
NM_000553.4(WRN):c.2312G>C (p.Cys771Ser) rs746161973
NM_000553.4(WRN):c.2361G>T (p.Leu787=) rs1800392
NM_000553.4(WRN):c.2529G>C (p.Lys843Asn) rs886062889
NM_000553.4(WRN):c.2537A>G (p.Glu846Gly) rs886062890
NM_000553.4(WRN):c.2735T>G (p.Ile912Ser) rs11574323
NM_000553.4(WRN):c.2959C>T (p.Arg987Ter) rs747319628
NM_000553.4(WRN):c.3000G>C (p.Arg1000Ser) rs886062891
NM_000553.4(WRN):c.3078A>G (p.Gly1026=) rs886062892
NM_000553.4(WRN):c.3138+6C>T rs3024239
NM_000553.4(WRN):c.3138+7G>A rs2737335
NM_000553.4(WRN):c.3139-1G>C rs113993961
NM_000553.4(WRN):c.3222G>T (p.Leu1074Phe) rs1801195
NM_000553.4(WRN):c.3236C>T (p.Ser1079Leu) rs3087414
NM_000553.4(WRN):c.3323A>C (p.Lys1108Thr) rs201274303
NM_000553.4(WRN):c.3343T>A (p.Cys1115Ser) rs886062893
NM_000553.4(WRN):c.3384-3T>C rs3087424
NM_000553.4(WRN):c.3785C>G (p.Thr1262Arg) rs78488552
NM_000553.4(WRN):c.3819+14T>C rs886062894
NM_000553.4(WRN):c.3972C>T (p.Pro1324=) rs370253199
NM_000553.4(WRN):c.4083C>T (p.Ser1361=) rs1801196
NM_000553.4(WRN):c.4099T>C (p.Cys1367Arg) rs1346044
NM_000553.4(WRN):c.4180A>G (p.Ile1394Val) rs545431480
NM_000553.4(WRN):c.725-3delT rs778493200
NM_000553.4(WRN):c.839+11delA rs886062886
NM_000553.5(WRN):c.*553dup rs777731812
NM_000553.5(WRN):c.-284dup rs886062882
NM_000553.5(WRN):c.-289dup rs886062880
NM_000553.5(WRN):c.-297dup rs886062878
NM_000553.5(WRN):c.-37A>G rs370014019
NM_000553.5(WRN):c.1149G>T (p.Leu383Phe) rs4987238
NM_000553.5(WRN):c.1155G>A (p.Glu385=) rs2230010
NM_000553.5(WRN):c.1161G>A (p.Met387Ile) rs1800391
NM_000553.5(WRN):c.1165del (p.Arg389Glufs) rs878854131
NM_000553.5(WRN):c.16T>C (p.Leu6=) rs202148988
NM_000553.5(WRN):c.1953C>T (p.Gly651=) rs11574263
NM_000553.5(WRN):c.1982-2A>G rs1563351045
NM_000553.5(WRN):c.2241T>G (p.Leu747=) rs2230011
NM_000553.5(WRN):c.2983G>A (p.Ala995Thr) rs140768346
NM_000553.5(WRN):c.3130dup (p.Thr1044Asnfs) rs1563376595
NM_000553.5(WRN):c.3139-9T>C rs377226126
NM_000553.5(WRN):c.340G>A (p.Val114Ile) rs2230009
NM_000553.5(WRN):c.355+4G>C rs145764920
NM_000553.5(WRN):c.3875C>A (p.Ser1292Tyr) rs142614369
NM_000553.5(WRN):c.421G>A (p.Glu141Lys) rs769317785
NM_000553.5(WRN):c.513C>T (p.Cys171=) rs1800389
NM_000553.5(WRN):c.839+25dup rs370040831
NM_000553.5(WRN):c.95A>G (p.Lys32Arg) rs34477820

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