ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.193C>G (p.Pro65Ala)

dbSNP: rs1429977258
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000514692 SCV000610481 uncertain significance not provided 2017-09-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000514692 SCV004639698 benign not provided 2023-12-07 criteria provided, single submitter clinical testing

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