ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.953-5T>C

gnomAD frequency: 0.00001  dbSNP: rs746073787
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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 RCV001441751 SCV001644687 likely benign Neuroblastoma, susceptibility to, 3 2023-06-16 criteria provided, single submitter clinical testing

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