ClinVar Miner

Submissions for variant NM_000381.4(MID1):c.1510T>C (p.Leu504=)

dbSNP: rs797045704
Minimum review status: Collection method:
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000192756 SCV000248044 uncertain significance not specified 2015-05-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002517100 SCV002930529 likely benign not provided 2024-09-23 criteria provided, single submitter clinical testing

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