ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.12012+97G>A

gnomAD frequency: 0.04274  dbSNP: rs78884140
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 RCV001639312 SCV001850511 benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001639312 SCV005310888 benign not provided criteria provided, single submitter not provided

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