ClinVar Miner

Submissions for variant NM_001377304.1(GFI1B):c.649-5G>C

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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 RCV003447740 SCV004175423 uncertain significance Platelet-type bleeding disorder 17 2020-11-17 criteria provided, single submitter clinical testing

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