ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.2204+8T>A

dbSNP: rs758076491
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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 RCV001359997 SCV001555888 likely benign Neuroblastoma, susceptibility to, 3 2023-08-14 criteria provided, single submitter clinical testing

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