ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3120G>A (p.Val1040=)

dbSNP: rs1553394893
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000589844 SCV000698290 likely benign not specified 2019-08-20 criteria provided, single submitter clinical testing
Invitae RCV001407422 SCV001609398 likely benign Neuroblastoma, susceptibility to, 3 2023-10-23 criteria provided, single submitter clinical testing

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