ClinVar Miner

Submissions for variant NM_002435.3(MPI):c.845-10G>C

dbSNP: rs748693066
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000982584 SCV001130600 likely benign MPI-congenital disorder of glycosylation 2023-10-22 criteria provided, single submitter clinical testing
Natera, Inc. RCV000982584 SCV001454930 uncertain significance MPI-congenital disorder of glycosylation 2020-03-11 no assertion criteria provided clinical testing

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