ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.78C>T (p.His26=) (rs746222481)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000635588 SCV000757007 likely benign Multiple fibrofolliculomas 2020-11-10 criteria provided, single submitter clinical testing
Ambry Genetics RCV001026930 SCV001189405 likely benign Hereditary cancer-predisposing syndrome 2015-08-18 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
GeneDx RCV001530782 SCV001745680 likely benign not provided 2018-12-28 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 25344691)

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