ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.13515-239C>G

gnomAD frequency: 0.12656  dbSNP: rs2960320
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001722737 SCV001949435 benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001722737 SCV005310895 benign not provided criteria provided, single submitter not provided

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