ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.871+16T>A (rs116643153)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000121109 SCV000532527 likely benign not specified 2017-12-19 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.
Biesecker Lab/Clinical Genomics Section,National Institutes of Health RCV000034794 SCV000043268 variant of unknown significance not provided 2012-07-13 no assertion criteria provided research Converted during submission to Uncertain significance.
ITMI RCV000121109 SCV000085277 not provided not specified 2013-09-19 no assertion provided reference population

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