ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.396+59T>C (rs41525346)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biesecker Lab/Clinical Genomics Section,National Institutes of Health RCV000034792 SCV000043270 no known pathogenicity not provided 2012-07-13 no assertion criteria provided research Converted during submission to Benign.
ITMI RCV000119849 SCV000083899 not provided not specified 2013-09-19 no assertion provided reference population

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