ClinVar Miner

Submissions for variant NM_001374828.1(ARID1B):c.6641T>C (p.Ile2214Thr)

gnomAD frequency: 0.00004  dbSNP: rs878852997
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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 RCV000224656 SCV000280727 likely benign not provided 2016-04-18 criteria provided, single submitter clinical testing Converted during submission to Likely benign.
Labcorp Genetics (formerly Invitae), Labcorp RCV000224656 SCV003278019 benign not provided 2023-12-11 criteria provided, single submitter clinical testing

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