ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.668-13T>C

gnomAD frequency: 0.00001  dbSNP: rs1158740527
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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 RCV002079740 SCV002421528 likely benign Neuroblastoma, susceptibility to, 3 2023-11-17 criteria provided, single submitter clinical testing

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