ClinVar Miner

Submissions for variant NM_153717.3(EVC):c.1563+1754G>A

gnomAD frequency: 0.01725  dbSNP: rs115269936
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001811611 SCV001159564 benign not provided 2023-11-06 criteria provided, single submitter clinical testing

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