ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.37C>T (p.Leu13=)

dbSNP: rs749730757
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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 RCV001435032 SCV001637850 likely benign Neuroblastoma, susceptibility to, 3 2020-01-16 criteria provided, single submitter clinical testing

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