ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.667+14G>T

gnomAD frequency: 0.00004  dbSNP: rs781586901
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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 RCV002217879 SCV002376689 likely benign Neuroblastoma, susceptibility to, 3 2023-11-10 criteria provided, single submitter clinical testing

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