ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.11609-133A>T

dbSNP: rs112148182
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001614062 SCV001837412 benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001614062 SCV005310877 benign not provided criteria provided, single submitter not provided

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