ClinVar Miner

Variants in gene WRN with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 14
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NM_000553.6(WRN):c.1149G>T (p.Leu383Phe) rs4987238
NM_000553.6(WRN):c.1530A>T (p.Glu510Asp) rs149565907
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.1909C>T (p.Arg637Trp) rs148286708
NM_000553.6(WRN):c.2342C>T (p.Thr781Ile) rs17847568
NM_000553.6(WRN):c.2500C>T (p.Arg834Cys) rs3087425
NM_000553.6(WRN):c.2983G>A (p.Ala995Thr) rs140768346
NM_000553.6(WRN):c.355+4G>C rs145764920
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.4180A>G (p.Ile1394Val) rs545431480
NM_000553.6(WRN):c.95A>G (p.Lys32Arg) rs34477820

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