ClinVar Miner

Submissions for variant NM_139242.4(MTFMT):c.1092A>G (p.Gln364=)

gnomAD frequency: 0.00050  dbSNP: rs4586374
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 RCV000964344 SCV000521488 likely benign not provided 2020-10-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000964344 SCV001111543 benign not provided 2024-10-10 criteria provided, single submitter clinical testing

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