ClinVar Miner

Submissions for variant NM_005612.5(REST):c.2326C>G (p.Pro776Ala)

gnomAD frequency: 0.01240  dbSNP: rs61748756
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001519630 SCV001728522 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001519630 SCV001768274 likely benign not provided 2022-04-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001519630 SCV005259602 likely benign not provided criteria provided, single submitter not provided

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