ClinVar Miner

Submissions for variant NM_005188.4(CBL):c.1008-18G>A

gnomAD frequency: 0.00006  dbSNP: rs764185548
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002155200 SCV002418176 likely benign RASopathy 2023-11-10 criteria provided, single submitter clinical testing

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