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:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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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