ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.197+23C>A

gnomAD frequency: 0.00365  dbSNP: rs202151374
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001811579 SCV001157572 benign not provided 2020-01-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001811579 SCV005308396 benign not provided criteria provided, single submitter not provided

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