ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.2976A>G (p.Val992=)

dbSNP: rs2148178556
Minimum review status: Collection method:
Minimum conflict level:
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 RCV001424984 SCV001627594 likely benign Neuroblastoma, susceptibility to, 3 2019-12-19 criteria provided, single submitter clinical testing

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