ClinVar Miner

Submissions for variant NM_001754.4(RUNX1):c.927C>T (p.Gly309=) (rs59802347)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000228598 SCV000435946 likely benign Familial platelet disorder with associated myeloid malignancy 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000228598 SCV000287194 benign Familial platelet disorder with associated myeloid malignancy 2018-01-10 criteria provided, single submitter clinical testing
PreventionGenetics RCV000680436 SCV000807807 likely benign not provided 2017-11-30 criteria provided, single submitter clinical testing

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