ClinVar Miner

Submissions for variant NM_001754.4(RUNX1):c.183G>A (p.Pro61=) (rs76558016)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory,University of Chicago RCV000194463 SCV000248755 benign not specified 2018-10-31 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000194463 SCV000308032 benign not specified 2016-08-01 criteria provided, single submitter clinical testing
Invitae RCV000471438 SCV000560767 benign Familial platelet disorder with associated myeloid malignancy 2019-12-31 criteria provided, single submitter clinical testing

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