ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.2583G>A (p.Leu861=)

gnomAD frequency: 0.00001  dbSNP: rs201079493
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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 RCV000952375 SCV001098874 likely benign Neuroblastoma, susceptibility to, 3 2024-01-02 criteria provided, single submitter clinical testing

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