ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.61G>A (p.Val21Met)

gnomAD frequency: 0.00001  dbSNP: rs1368307834
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001925126 SCV002173931 uncertain significance Werner syndrome 2021-08-31 criteria provided, single submitter clinical testing

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