ClinVar Miner

Submissions for variant NM_002392.6(MDM2):c.14+55C>T

gnomAD frequency: 0.29629  dbSNP: rs2870820
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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 RCV001520940 SCV001730157 benign Accelerated tumor formation, susceptibility to 2025-01-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705792 SCV005216116 likely benign not provided criteria provided, single submitter not provided

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