ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.4404G>A (p.Gly1468=)

dbSNP: rs1256422825
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001484874 SCV001689297 likely benign Neuroblastoma, susceptibility to, 3 2022-07-12 criteria provided, single submitter clinical testing

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