ClinVar Miner

Submissions for variant NM_000214.3(JAG1):c.-386dup

dbSNP: rs886056519
Minimum review status: Collection method:
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000294874 SCV000432979 uncertain significance Arteriohepatic dysplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000352200 SCV000432980 uncertain significance Isolated Nonsyndromic Congenital Heart Disease 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001691963 SCV001911850 benign not provided 2021-02-03 criteria provided, single submitter clinical testing

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