ClinVar Miner

Submissions for variant NM_004530.6(MMP2):c.105C>T (p.Ile35=)

gnomAD frequency: 0.00002  dbSNP: rs764055331
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000173346 SCV000224446 uncertain significance not provided 2015-02-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000173346 SCV002415963 likely benign not provided 2024-09-21 criteria provided, single submitter clinical testing

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