ClinVar Miner

Submissions for variant NM_001036.5(RYR3):c.9290T>G (p.Val3097Gly) (rs1555456665)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000622507 SCV000742402 uncertain significance Inborn genetic diseases 2017-07-05 criteria provided, single submitter clinical testing
GenomeConnect, ClinGen RCV001175274 SCV001338875 not provided not provided no assertion provided phenotyping only Variant interpretted as Uncertain significance and reported on 08-01-2017 by Lab or GTR ID 61756. GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant.

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