ClinVar Miner

Submissions for variant NM_001374828.1(ARID1B):c.2211G>A (p.Leu737=)

dbSNP: rs797045271
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000194166 SCV000246506 uncertain significance not specified 2015-08-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005055694 SCV005717493 likely benign not provided 2024-09-28 criteria provided, single submitter clinical testing

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