ClinVar Miner

Submissions for variant NM_015450.3(POT1):c.1793-12T>C

gnomAD frequency: 0.00001  dbSNP: rs777834542
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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 RCV002178752 SCV002477686 likely benign Tumor predisposition syndrome 3 2024-01-11 criteria provided, single submitter clinical testing

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