ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.4260G>T (p.Gly1420=)

dbSNP: rs2148138882
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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 RCV002198661 SCV002485608 likely benign Neuroblastoma, susceptibility to, 3 2021-01-07 criteria provided, single submitter clinical testing

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