ClinVar Miner

Submissions for variant NM_005373.3(MPL):c.1359G>A (p.Pro453=)

dbSNP: rs1262936822
Minimum review status: Collection method:
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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 RCV001469287 SCV001673366 likely benign Congenital amegakaryocytic thrombocytopenia; Essential thrombocythemia 2022-07-24 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001820162 SCV002068951 uncertain significance not specified 2018-03-22 criteria provided, single submitter clinical testing

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