ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.921T>G (p.Pro307=)

dbSNP: rs1391544676
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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 RCV001490403 SCV001694964 likely benign Neuroblastoma, susceptibility to, 3 2020-08-15 criteria provided, single submitter clinical testing

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