ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.897C>T (p.Ser299=)

dbSNP: rs1389708232
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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 RCV001506391 SCV001711313 likely benign Neuroblastoma, susceptibility to, 3 2019-07-26 criteria provided, single submitter clinical testing

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