ClinVar Miner

Submissions for variant NM_007289.4(MME):c.924C>A (p.Ile308=)

gnomAD frequency: 0.00009  dbSNP: rs150252105
Minimum review status: Collection method:
Minimum conflict level:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002109117 SCV002439100 likely benign not provided 2023-06-02 criteria provided, single submitter clinical testing

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