ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.871+7C>A

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005140640 SCV005761103 likely benign Birt-Hogg-Dube syndrome 2024-10-07 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005249779 SCV005899198 likely benign Birt-Hogg-Dube syndrome 1 2024-10-23 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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