ClinVar Miner

Submissions for variant NM_004958.4(MTOR):c.3655-281A>G

gnomAD frequency: 0.63053  dbSNP: rs1010447
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 RCV001654652 SCV001868162 benign not provided 2018-07-06 criteria provided, single submitter clinical testing

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