ClinVar Miner

Submissions for variant NM_000129.4(F13A1):c.798+2T>C

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Praxis fuer Humangenetik Tuebingen RCV001092974 SCV001249735 pathogenic not provided 2019-10-01 criteria provided, single submitter clinical testing
Center for Genomic Medicine,King Faisal Specialist Hospital and Research Center RCV001420448 SCV001622484 pathogenic Factor XIII, A subunit, deficiency of 2021-04-28 criteria provided, single submitter research

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