ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.1809G>T (p.Val603=)

dbSNP: rs141025125
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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 RCV001462648 SCV001666572 likely benign Neuroblastoma, susceptibility to, 3 2018-02-28 criteria provided, single submitter clinical testing

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