ClinVar Miner

Submissions for variant NM_003070.5(SMARCA2):c.4737+18G>A

gnomAD frequency: 0.00026  dbSNP: rs191731237
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001680154 SCV001899813 benign not provided 2021-01-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001680154 SCV002351407 benign not provided 2025-01-13 criteria provided, single submitter clinical testing

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