ClinVar Miner

Submissions for variant NM_004958.4(MTOR):c.4278G>A (p.Pro1426=)

dbSNP: rs764725826
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 RCV001422482 SCV001625033 likely benign not provided 2025-01-27 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004782735 SCV005394920 likely benign not specified 2024-09-11 criteria provided, single submitter clinical testing

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