ClinVar Miner

Submissions for variant NM_003070.5(SMARCA2):c.1522-19G>A

gnomAD frequency: 0.00509  dbSNP: rs141618610
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001544998 SCV001764234 likely benign not provided 2018-10-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001544998 SCV002410819 benign not provided 2025-01-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001544998 SCV005225262 likely benign not provided criteria provided, single submitter not provided

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