ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.1176+14T>A

gnomAD frequency: 0.00001  dbSNP: rs757366854
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000249390 SCV000316053 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058406 SCV002423768 likely benign Birt-Hogg-Dube syndrome 2024-11-05 criteria provided, single submitter clinical testing

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