ClinVar Miner

Submissions for variant NM_005188.4(CBL):c.*7578TC[1]

dbSNP: rs376134331
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000327907 SCV000367898 benign Noonan-like syndrome 2016-06-14 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV001813455 SCV002060483 likely benign Noonan syndrome and Noonan-related syndrome 2016-12-22 criteria provided, single submitter clinical testing

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