ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.2268C>T (p.Phe756=)

dbSNP: rs1555770357
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000655696 SCV000777627 likely benign RYR1-related disorder 2023-11-20 criteria provided, single submitter clinical testing

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