ClinVar Miner

Submissions for variant NM_024408.4(NOTCH2):c.5479+46A>G

gnomAD frequency: 0.00048  dbSNP: rs200559571
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001717800 SCV001945853 benign not provided 2020-07-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001717800 SCV005283286 benign not provided criteria provided, single submitter not provided

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