ClinVar Miner

Submissions for variant NM_005188.4(CBL):c.*559_*560insCAA

dbSNP: rs3833768
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
Illumina Laboratory Services, Illumina RCV000324954 SCV000367789 uncertain significance Noonan-like syndrome 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004692992 SCV005191458 uncertain significance not provided criteria provided, single submitter not provided

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