ClinVar Miner

Submissions for variant NM_015450.3(POT1):c.654A>T (p.Ile218=)

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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 RCV002598053 SCV002955815 likely benign Tumor predisposition syndrome 3 2022-01-19 criteria provided, single submitter clinical testing

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