ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3646-13T>C

dbSNP: rs2148159628
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002140879 SCV002463395 likely benign Neuroblastoma, susceptibility to, 3 2024-01-06 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256935 SCV002528487 uncertain significance Hereditary cancer-predisposing syndrome 2021-09-23 criteria provided, single submitter curation

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