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: 11
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HGVS dbSNP
NM_000553.4(WRN):c.1530A>T (p.Glu510Asp) rs149565907
NM_000553.4(WRN):c.3422C>T (p.Ser1141Leu) rs139323683
NM_000553.4(WRN):c.3785C>G (p.Thr1262Arg) rs78488552
NM_000553.5(WRN):c.1149G>T (p.Leu383Phe) rs4987238
NM_000553.5(WRN):c.16T>C (p.Leu6=) rs202148988
NM_000553.5(WRN):c.1953C>T (p.Gly651=) rs11574263
NM_000553.5(WRN):c.2241T>G (p.Leu747=) rs2230011
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.355+4G>C rs145764920
NM_000553.5(WRN):c.95A>G (p.Lys32Arg) rs34477820

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