ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.2915-9T>C

gnomAD frequency: 0.00144  dbSNP: rs373765395
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000457734 SCV000554760 benign Neuroblastoma, susceptibility to, 3 2025-02-03 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000457734 SCV000602467 benign Neuroblastoma, susceptibility to, 3 2023-11-22 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002257729 SCV002528445 benign Hereditary cancer-predisposing syndrome 2021-06-13 criteria provided, single submitter curation
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000508380 SCV003929358 benign not specified 2023-04-22 criteria provided, single submitter clinical testing

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