ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.720G>A (p.Ser240=) (rs186366202)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000573098 SCV000673415 likely benign Hereditary cancer-predisposing syndrome 2017-04-10 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
GeneDx RCV000842492 SCV000984515 likely benign not provided 2020-09-27 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 27149842)
Invitae RCV001084076 SCV001010196 likely benign Multiple fibrofolliculomas 2020-10-19 criteria provided, single submitter clinical testing

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