ClinVar Miner

Submissions for variant NM_004958.4(MTOR):c.6004A>G (p.Ser2002Gly)

dbSNP: rs2100413071
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001515915 SCV001724097 benign not provided 2020-03-20 criteria provided, single submitter clinical testing

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