ClinVar Miner

Submissions for variant NM_005188.3(CBL):c.-127_-125GGC[8]

dbSNP: rs57028199
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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 RCV000402775 SCV000367739 uncertain significance Noonan-like syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001690003 SCV001907108 benign not provided 2019-08-15 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV001813451 SCV002060723 uncertain significance Noonan syndrome and Noonan-related syndrome 2017-01-30 criteria provided, single submitter clinical testing

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