ClinVar Miner

Submissions for variant NM_001715.3(BLK):c.952+46C>A

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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 RCV003436735 SCV004164364 benign not provided 2022-04-01 criteria provided, single submitter clinical testing BLK: BS1, BS2

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