ClinVar Miner

Submissions for variant NM_024408.4(NOTCH2):c.4006-54A>G

gnomAD frequency: 0.01227  dbSNP: rs6658796
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 RCV001564295 SCV001787442 likely benign not provided 2018-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001564295 SCV005261576 likely benign not provided criteria provided, single submitter not provided

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