ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.787+14T>G

dbSNP: rs1394439148
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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 RCV002087108 SCV002320908 likely benign Neuroblastoma, susceptibility to, 3 2021-03-10 criteria provided, single submitter clinical testing

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