ClinVar Miner

Submissions for variant NM_004958.4(MTOR):c.7367-9T>C

gnomAD frequency: 0.00001  dbSNP: rs780630255
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000864571 SCV001005389 likely benign not provided 2024-11-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000864571 SCV005261222 likely benign not provided criteria provided, single submitter not provided

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