ClinVar Miner

Submissions for variant NM_004958.4(MTOR):c.7227G>A (p.Glu2409=)

dbSNP: rs1570907484
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000936836 SCV001082609 likely benign not provided 2020-03-07 criteria provided, single submitter clinical testing

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