ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.2091C>A (p.Thr697=)

dbSNP: rs1252650401
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 RCV002119415 SCV002395261 likely benign Neuroblastoma, susceptibility to, 3 2021-05-29 criteria provided, single submitter clinical testing

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