ClinVar Miner

Submissions for variant NM_004958.4(MTOR):c.6663-88dup

dbSNP: rs377227945
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001617062 SCV001838454 benign not provided 2019-08-10 criteria provided, single submitter clinical testing

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