ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3873G>T (p.Leu1291=)

gnomAD frequency: 0.00001  dbSNP: rs772093140
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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 RCV001453888 SCV001657597 likely benign Neuroblastoma, susceptibility to, 3 2019-02-14 criteria provided, single submitter clinical testing

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