ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.3125C>T (p.Ala1042Val)

dbSNP: rs759240091
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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 RCV001459533 SCV001663375 likely benign Werner syndrome 2020-08-03 criteria provided, single submitter clinical testing

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