ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.2816-7T>C

dbSNP: rs755251438
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000234630 SCV000288338 likely benign Neuroblastoma, susceptibility to, 3 2023-11-27 criteria provided, single submitter clinical testing
GeneDx RCV003128608 SCV003805754 likely benign not provided 2018-08-02 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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