ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3642C>G (p.Arg1214=)

dbSNP: rs1394591243
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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 RCV001473954 SCV001678117 likely benign Neuroblastoma, susceptibility to, 3 2019-12-06 criteria provided, single submitter clinical testing

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