ClinVar Miner

Variants in gene WRN with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 18
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HGVS dbSNP
NM_000553.4(WRN):c.1530A>T (p.Glu510Asp) rs149565907
NM_000553.4(WRN):c.1577-3C>A rs3087409
NM_000553.4(WRN):c.2361G>T (p.Leu787=) rs1800392
NM_000553.4(WRN):c.2950T>A (p.Leu984Ile) rs146443310
NM_000553.4(WRN):c.3138+6C>T rs3024239
NM_000553.4(WRN):c.3138+7G>A rs2737335
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.3384-3T>C rs3087424
NM_000553.4(WRN):c.4083C>T (p.Ser1361=) rs1801196
NM_000553.4(WRN):c.4099T>C (p.Cys1367Arg) rs1346044
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.2983G>A (p.Ala995Thr) rs140768346
NM_000553.5(WRN):c.340G>A (p.Val114Ile) rs2230009
NM_000553.5(WRN):c.720T>G (p.Asn240Lys) rs148229804
NM_000553.5(WRN):c.970A>G (p.Thr324Ala) rs1800390

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