ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.2632+17G>A

gnomAD frequency: 0.00008  dbSNP: rs201350160
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002099269 SCV002433363 likely benign Neuroblastoma, susceptibility to, 3 2023-12-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002099269 SCV002808967 likely benign Neuroblastoma, susceptibility to, 3 2022-05-18 criteria provided, single submitter clinical testing

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