ClinVar Miner

Submissions for variant NM_001754.5(RUNX1):c.1256T>G (p.Val419Gly)

dbSNP: rs2056452215
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003132370 SCV003814341 uncertain significance not provided 2022-01-06 criteria provided, single submitter clinical testing
Birmingham Platelet Group; University of Birmingham RCV001270549 SCV001450848 likely pathogenic Abnormal bleeding; Thrombocytopenia 2020-05-01 no assertion criteria provided research

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