ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.4839T>C (p.Asn1613=)

dbSNP: rs1487769564
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001430784 SCV001633529 likely benign Neuroblastoma, susceptibility to, 3 2020-03-31 criteria provided, single submitter clinical testing

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