ClinVar Miner

Submissions for variant NM_001374828.1(ARID1B):c.2655G>A (p.Ser885=)

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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 RCV002917517 SCV003247581 benign not provided 2022-07-13 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002917517 SCV004701848 likely benign not provided 2024-01-01 criteria provided, single submitter clinical testing ARID1B: BP4, BP7

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