ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.207G>A (p.Arg69=)

dbSNP: rs1553380407
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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 RCV000547175 SCV000648642 likely benign Neuroblastoma, susceptibility to, 3 2021-08-16 criteria provided, single submitter clinical testing

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