ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.2118_2119del (p.Ser707fs)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV004573867 SCV005055840 likely pathogenic Werner syndrome 2023-12-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV004573867 SCV005676860 likely pathogenic Werner syndrome 2024-03-28 criteria provided, single submitter clinical testing

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