ClinVar Miner

Submissions for variant NM_007289.4(MME):c.1590G>A (p.Val530=)

gnomAD frequency: 0.00001  dbSNP: rs1209332250
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002124115 SCV002450860 likely benign not provided 2024-07-21 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV002124115 SCV003808863 uncertain significance not provided 2022-09-08 criteria provided, single submitter clinical testing

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