ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.886G>A (p.Glu296Lys)

dbSNP: rs56077855
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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 RCV000647483 SCV000769279 likely benign Neuroblastoma, susceptibility to, 3 2024-01-19 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256447 SCV002528545 benign Hereditary cancer-predisposing syndrome 2021-12-16 criteria provided, single submitter curation

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