ClinVar Miner

List of variants in gene WRN reported as benign for Werner syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 57
Download table as spreadsheet
HGVS dbSNP
NM_000553.4(WRN):c.-278G>C rs11574157
NM_000553.4(WRN):c.-408C>T rs11574156
NM_000553.4(WRN):c.-618C>G rs7017069
NM_000553.6(WRN):c.*570A>G rs11574415
NM_000553.6(WRN):c.-163C>G rs11574160
NM_000553.6(WRN):c.-213G>A rs11574158
NM_000553.6(WRN):c.1149G>T (p.Leu383Phe) rs4987238
NM_000553.6(WRN):c.1155G>A (p.Glu385=) rs2230010
NM_000553.6(WRN):c.1161G>A (p.Met387Ile) rs1800391
NM_000553.6(WRN):c.1247A>G (p.Asp416Gly) rs560922465
NM_000553.6(WRN):c.1350+3A>G rs182813211
NM_000553.6(WRN):c.1378G>A (p.Asp460Asn) rs556958354
NM_000553.6(WRN):c.144A>G (p.Glu48=) rs145959045
NM_000553.6(WRN):c.1530A>T (p.Glu510Asp) rs149565907
NM_000553.6(WRN):c.1577-3C>A rs3087409
NM_000553.6(WRN):c.16T>C (p.Leu6=) rs202148988
NM_000553.6(WRN):c.1717A>G (p.Thr573Ala) rs150148567
NM_000553.6(WRN):c.1725T>C (p.Tyr575=) rs13438802
NM_000553.6(WRN):c.1788T>C (p.Ser596=) rs13438803
NM_000553.6(WRN):c.1882C>G (p.Leu628Val) rs77969734
NM_000553.6(WRN):c.1909C>T (p.Arg637Trp) rs148286708
NM_000553.6(WRN):c.1953C>T (p.Gly651=) rs11574263
NM_000553.6(WRN):c.1982-5del rs397723919
NM_000553.6(WRN):c.1982-6_1982-5del rs397723919
NM_000553.6(WRN):c.2241T>G (p.Leu747=) rs2230011
NM_000553.6(WRN):c.2342C>T (p.Thr781Ile) rs17847568
NM_000553.6(WRN):c.2361G>T (p.Leu787=) rs1800392
NM_000553.6(WRN):c.2500C>T (p.Arg834Cys) rs3087425
NM_000553.6(WRN):c.2630+10dup rs747115098
NM_000553.6(WRN):c.2937T>G (p.Ile979Met) rs147802438
NM_000553.6(WRN):c.2950T>A (p.Leu984Ile) rs146443310
NM_000553.6(WRN):c.2983G>A (p.Ala995Thr) rs140768346
NM_000553.6(WRN):c.3138+6C>T rs3024239
NM_000553.6(WRN):c.3138+7G>A rs2737335
NM_000553.6(WRN):c.3222G>T (p.Leu1074Phe) rs1801195
NM_000553.6(WRN):c.3236C>T (p.Ser1079Leu) rs3087414
NM_000553.6(WRN):c.3237G>A (p.Ser1079=) rs11574345
NM_000553.6(WRN):c.3384-3T>C rs3087424
NM_000553.6(WRN):c.340G>A (p.Val114Ile) rs2230009
NM_000553.6(WRN):c.3422C>T (p.Ser1141Leu) rs139323683
NM_000553.6(WRN):c.3453G>A (p.Glu1151=) rs144116311
NM_000553.6(WRN):c.355+4G>C rs145764920
NM_000553.6(WRN):c.3627T>A (p.Ala1209=) rs780963410
NM_000553.6(WRN):c.3785C>G (p.Thr1262Arg) rs78488552
NM_000553.6(WRN):c.3875C>A (p.Ser1292Tyr) rs142614369
NM_000553.6(WRN):c.3900C>A (p.Pro1300=) rs138886038
NM_000553.6(WRN):c.4015G>A (p.Val1339Ile) rs11574395
NM_000553.6(WRN):c.4083C>T (p.Ser1361=) rs1801196
NM_000553.6(WRN):c.4099T>C (p.Cys1367Arg) rs1346044
NM_000553.6(WRN):c.4180A>G (p.Ile1394Val) rs545431480
NM_000553.6(WRN):c.4216C>T (p.Arg1406Ter) rs11574410
NM_000553.6(WRN):c.4248T>C (p.Asp1416=) rs112024742
NM_000553.6(WRN):c.513C>T (p.Cys171=) rs1800389
NM_000553.6(WRN):c.720T>G (p.Asn240Lys) rs148229804
NM_000553.6(WRN):c.839+25del rs370040831
NM_000553.6(WRN):c.95A>G (p.Lys32Arg) rs34477820
NM_000553.6(WRN):c.970A>G (p.Thr324Ala) rs1800390

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.