ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.2190C>T (p.Ala730=)

dbSNP: rs2148197228
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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 RCV001467081 SCV001671099 likely benign Neuroblastoma, susceptibility to, 3 2022-11-01 criteria provided, single submitter clinical testing

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