ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3300C>G (p.Gly1100=)

dbSNP: rs752819935
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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 RCV001485327 SCV001689759 likely benign Neuroblastoma, susceptibility to, 3 2020-03-11 criteria provided, single submitter clinical testing

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