ClinVar Miner

Submissions for variant NM_139242.4(MTFMT):c.646-18dup

dbSNP: rs372515409
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
GeneDx RCV000676586 SCV001896363 benign not provided 2019-08-09 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000676586 SCV000802373 benign not provided 2016-02-29 no assertion criteria provided clinical testing

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