ClinVar Miner

Submissions for variant NM_015450.3(POT1):c.561C>G (p.Thr187=)

dbSNP: rs1293186024
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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 RCV001392968 SCV001594617 likely benign Tumor predisposition syndrome 3 2024-10-30 criteria provided, single submitter clinical testing

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