ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.376-13C>T

dbSNP: rs2073407612
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001177568 SCV001341800 likely benign Hereditary cancer-predisposing syndrome 2018-05-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003769909 SCV004615374 likely benign Li-Fraumeni syndrome 2023-07-07 criteria provided, single submitter clinical testing
Laboratory of Virology, Oncology, Biosciences and Environment, Faculty of Sciences and Techniques, Mohammedia- University Hassan II of Casablanca RCV003483783 SCV004232155 uncertain significance Prostate cancer, hereditary, 1 2024-01-01 no assertion criteria provided clinical testing

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