ClinVar Miner

Submissions for variant NM_014975.3(MAST1):c.1366+2874T>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003421845 SCV004137912 benign not provided 2022-05-01 criteria provided, single submitter clinical testing MAST1: BS1, BS2

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