ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3948A>G (p.Gly1316=)

dbSNP: rs2148143639
Minimum review status: Collection method:
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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 RCV001499977 SCV001704752 likely benign Neuroblastoma, susceptibility to, 3 2020-10-20 criteria provided, single submitter clinical testing

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