ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.75-19T>A

dbSNP: rs2073508941
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002179794 SCV002337502 likely benign Li-Fraumeni syndrome 2023-08-11 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268601 SCV002551191 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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