ClinVar Miner

Submissions for variant NM_000419.5(ITGA2B):c.2761T>C (p.Cys921Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
KardioGenetik, Herz- und Diabeteszentrum NRW RCV003391167 SCV004101818 uncertain significance Glanzmann thrombasthenia 1 2023-09-15 criteria provided, single submitter clinical testing

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