ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.993A>G (p.Lys331=)

dbSNP: rs1813285811
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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 RCV001492262 SCV001696870 likely benign Werner syndrome 2023-10-13 criteria provided, single submitter clinical testing

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