ClinVar Miner

Submissions for variant NM_020975.6(RET):c.2608-147C>T

gnomAD frequency: 0.17019  dbSNP: rs11238441
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000836540 SCV000978385 benign not provided 2018-06-20 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.
Genetics and Molecular Pathology, SA Pathology RCV002466593 SCV002761366 benign Multiple endocrine neoplasia, type 2 2019-08-06 criteria provided, single submitter clinical testing

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