ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.667+11C>A

dbSNP: rs765124982
Minimum review status: Collection method:
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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 RCV002212405 SCV002360723 likely benign Neuroblastoma, susceptibility to, 3 2023-12-30 criteria provided, single submitter clinical testing

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