ClinVar Miner

Submissions for variant NM_005188.3(CBL):c.-126_-125insTGG

dbSNP: rs878976124
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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 RCV000303771 SCV000367740 uncertain significance Noonan-like syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001723888 SCV001950711 benign not provided 2019-08-19 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV001813452 SCV002060726 uncertain significance Noonan syndrome and Noonan-related syndrome 2017-01-17 criteria provided, single submitter clinical testing

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