ClinVar Miner

Submissions for variant NM_002392.6(MDM2):c.14+309T>G

gnomAD frequency: 0.30651  dbSNP: rs2279744
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000014918 SCV001730158 benign Accelerated tumor formation, susceptibility to 2023-12-06 criteria provided, single submitter clinical testing
OMIM RCV000014918 SCV000035174 risk factor Accelerated tumor formation, susceptibility to 2009-10-01 no assertion criteria provided literature only

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