ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.1078A>C (p.Arg360=)

dbSNP: rs2148158589
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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 RCV001402367 SCV001604213 likely benign Neuroblastoma, susceptibility to, 3 2022-12-20 criteria provided, single submitter clinical testing

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