ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.4563C>T (p.Pro1521=)

gnomAD frequency: 0.00058  dbSNP: rs149095176
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001613531 SCV001834262 benign not provided 2020-03-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001613531 SCV003262306 benign not provided 2025-01-02 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001613531 SCV004123605 likely benign not provided 2023-02-01 criteria provided, single submitter clinical testing ARID1A: BP4, BP7, BS1

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