ClinVar Miner

Submissions for variant NM_002435.3(MPI):c.288C>T (p.Phe96=)

dbSNP: rs2064726439
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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 RCV001413348 SCV001615460 likely benign MPI-congenital disorder of glycosylation 2020-12-27 criteria provided, single submitter clinical testing

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