ClinVar Miner

Submissions for variant NM_001129820.2(SLFN14):c.2637del (p.Ser880fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Molecular Pathology, SA Pathology RCV002466891 SCV002761760 uncertain significance Platelet-type bleeding disorder 20 2021-09-03 criteria provided, single submitter clinical testing

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