ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.4947A>G (p.Thr1649=)

gnomAD frequency: 0.00004  dbSNP: rs201700725
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001557744 SCV001779561 likely benign not provided 2020-04-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001557744 SCV004684673 benign not provided 2024-01-11 criteria provided, single submitter clinical testing

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