ClinVar Miner

Submissions for variant NM_152743.4(BRAT1):c.1988G>A (p.Gly663Asp)

gnomAD frequency: 0.04216  dbSNP: rs61627394
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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 RCV001515791 SCV001723947 benign Neonatal-onset encephalopathy with rigidity and seizures 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001655752 SCV001869227 benign not provided 2018-07-21 criteria provided, single submitter clinical testing

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