ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.6166+10A>G

gnomAD frequency: 0.00001  dbSNP: rs776614601
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000435760 SCV000521772 likely benign not specified 2015-12-03 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV002519536 SCV003504992 uncertain significance Catecholaminergic polymorphic ventricular tachycardia 1 2023-05-15 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site. ClinVar contains an entry for this variant (Variation ID: 382018). This variant has not been reported in the literature in individuals affected with RYR2-related conditions. This variant is present in population databases (rs776614601, gnomAD no frequency). This sequence change falls in intron 40 of the RYR2 gene. It does not directly change the encoded amino acid sequence of the RYR2 protein.

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