ClinVar Miner

Submissions for variant NM_004994.3(MMP9):c.1896C>T (p.Leu632=)

gnomAD frequency: 0.00092  dbSNP: rs202160464
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
Eurofins Ntd Llc (ga) RCV000299784 SCV000341453 uncertain significance not provided 2017-04-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000299784 SCV001044589 benign not provided 2024-01-12 criteria provided, single submitter clinical testing

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