ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.2204+15G>C

gnomAD frequency: 0.00035  dbSNP: rs200910314
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 RCV002124656 SCV002409590 benign Neuroblastoma, susceptibility to, 3 2025-01-20 criteria provided, single submitter clinical testing

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