ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.2204+14A>T

dbSNP: rs778407286
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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 RCV002111493 SCV002392308 likely benign Neuroblastoma, susceptibility to, 3 2023-04-14 criteria provided, single submitter clinical testing

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