ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.1155-20_1155-19del

dbSNP: rs140451928
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000616106 SCV000729759 benign not specified 2017-06-09 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV002066724 SCV002406108 benign Neuroblastoma, susceptibility to, 3 2024-02-01 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV002066724 SCV004564841 benign Neuroblastoma, susceptibility to, 3 2023-09-18 criteria provided, single submitter clinical testing

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