ClinVar Miner

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

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 13
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HGVS dbSNP
NM_000553.4(WRN):c.1530A>T (p.Glu510Asp) rs149565907
NM_000553.4(WRN):c.1717A>G (p.Thr573Ala) rs150148567
NM_000553.4(WRN):c.2067C>T (p.Ser689=) rs191757062
NM_000553.4(WRN):c.2735T>G (p.Ile912Ser) rs11574323
NM_000553.4(WRN):c.2784A>G (p.Gly928=) rs755729832
NM_000553.4(WRN):c.3972C>T (p.Pro1324=) rs370253199
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.2983G>A (p.Ala995Thr) rs140768346
NM_000553.5(WRN):c.3139-9T>C rs377226126
NM_000553.5(WRN):c.3453G>A (p.Glu1151=) rs144116311
NM_000553.5(WRN):c.4035G>A (p.Thr1345=) rs767115441
NM_000553.5(WRN):c.747C>T (p.Asp249=) rs374142752

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