ClinVar Miner

Submissions for variant NM_015450.3(POT1):c.903G>C (p.Gln301His)

dbSNP: rs116916706
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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 RCV001392227 SCV001593868 likely benign Tumor predisposition syndrome 3 2024-07-03 criteria provided, single submitter clinical testing

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