ClinVar Miner

Submissions for variant NM_005373.3(MPL):c.1365_1366del (p.Arg456fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005016056 SCV005650857 likely pathogenic Primary myelofibrosis; Thrombocythemia 2; Congenital amegakaryocytic thrombocytopenia 1 2024-06-19 criteria provided, single submitter clinical testing

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