ClinVar Miner

List of variants in gene WRN reported as not provided for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
Download table as spreadsheet
HGVS dbSNP
NM_000553.4(WRN):c.1240C>G (p.Leu414Val) rs587778755
NM_000553.4(WRN):c.1530A>T (p.Glu510Asp) rs149565907
NM_000553.4(WRN):c.1708G>C (p.Val570Leu) rs587778746
NM_000553.4(WRN):c.1835C>G (p.Ser612Cys) rs11574250
NM_000553.4(WRN):c.2165A>G (p.Asn722Ser) rs186693124
NM_000553.4(WRN):c.2937T>G (p.Ile979Met) rs147802438
NM_000553.4(WRN):c.2950T>A (p.Leu984Ile) rs146443310
NM_000553.4(WRN):c.2978G>A (p.Arg993His) rs370713742
NM_000553.4(WRN):c.2986G>A (p.Asp996Asn) rs138379977
NM_000553.4(WRN):c.3097C>T (p.Arg1033Trp) rs143954702
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.3251C>T (p.Ser1084Leu) rs587778748
NM_000553.4(WRN):c.3422C>T (p.Ser1141Leu) rs139323683
NM_000553.4(WRN):c.3731C>T (p.Thr1244Met) rs370299361
NM_000553.4(WRN):c.3785C>G (p.Thr1262Arg) rs78488552
NM_000553.4(WRN):c.4099T>C (p.Cys1367Arg) rs1346044
NM_000553.4(WRN):c.4127C>T (p.Pro1376Leu) rs146055899
NM_000553.4(WRN):c.4165A>G (p.Lys1389Glu) rs587778751
NM_000553.4(WRN):c.587G>A (p.Arg196His) rs561603992
NM_000553.4(WRN):c.667A>G (p.Ile223Val) rs587778754
NM_000553.4(WRN):c.968C>T (p.Ser323Leu) rs369277330
NM_000553.5(WRN):c.107G>A (p.Arg36Gln) rs34084741
NM_000553.5(WRN):c.1149G>T (p.Leu383Phe) rs4987238
NM_000553.5(WRN):c.1161G>A (p.Met387Ile) rs1800391
NM_000553.5(WRN):c.1413A>C (p.Leu471Phe) rs587778745
NM_000553.5(WRN):c.145T>A (p.Phe49Ile) rs587778749
NM_000553.5(WRN):c.1762G>A (p.Val588Ile) rs587778747
NM_000553.5(WRN):c.1882C>G (p.Leu628Val) rs77969734
NM_000553.5(WRN):c.1909C>T (p.Arg637Trp) rs148286708
NM_000553.5(WRN):c.2500C>T (p.Arg834Cys) rs3087425
NM_000553.5(WRN):c.2983G>A (p.Ala995Thr) rs140768346
NM_000553.5(WRN):c.340G>A (p.Val114Ile) rs2230009
NM_000553.5(WRN):c.3506A>G (p.Asn1169Ser) rs587778750
NM_000553.5(WRN):c.3875C>A (p.Ser1292Tyr) rs142614369
NM_000553.5(WRN):c.4015G>A (p.Val1339Ile) rs11574395
NM_000553.5(WRN):c.4051G>A (p.Ala1351Thr) rs587778752
NM_000553.5(WRN):c.4191G>A (p.Glu1397=) rs369276959
NM_000553.5(WRN):c.4216C>T (p.Arg1406Ter) rs11574410
NM_000553.5(WRN):c.443T>A (p.Leu148Gln) rs587778753
NM_000553.5(WRN):c.514A>C (p.Thr172Pro) rs367991517
NM_000553.5(WRN):c.720T>G (p.Asn240Lys) rs148229804
NM_000553.5(WRN):c.95A>G (p.Lys32Arg) rs34477820
NM_000553.5(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.