ClinVar Miner

Submissions for variant NM_001036.6(RYR3):c.8705+17A>C

gnomAD frequency: 0.00508  dbSNP: rs148404688
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000514190 SCV000610626 likely benign not provided 2017-08-02 criteria provided, single submitter clinical testing

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