ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.2793-115C>G

dbSNP: rs7257550
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 RCV001667077 SCV001887769 benign not provided 2019-09-25 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001667077 SCV005315462 benign not provided criteria provided, single submitter not provided

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