ClinVar Miner

Submissions for variant NM_030973.3(MED25):c.1482+19G>A (rs4802632)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001001865 SCV001159582 benign Basel-Vanagaite-Smirin-Yosef syndrome 2020-06-11 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001173685 SCV001336787 benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing
GeneDx RCV001713062 SCV001941028 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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