ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3537T>C (p.Ile1179=)

dbSNP: rs2148166662
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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 RCV001445845 SCV001648883 likely benign Neuroblastoma, susceptibility to, 3 2019-02-14 criteria provided, single submitter clinical testing

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