ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.2356-16del

gnomAD frequency: 0.00002  dbSNP: rs752838625
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002172641 SCV002337968 likely benign Neuroblastoma, susceptibility to, 3 2024-02-06 criteria provided, single submitter clinical testing

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