ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.619-8C>T

gnomAD frequency: 0.00001  dbSNP: rs1274815686
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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 RCV001405454 SCV001607375 likely benign Birt-Hogg-Dube syndrome 2023-07-07 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002499868 SCV002809006 likely benign Birt-Hogg-Dube syndrome; Familial spontaneous pneumothorax; Potocki-Lupski syndrome; Nonpapillary renal cell carcinoma; Colorectal cancer 2022-04-27 criteria provided, single submitter clinical testing

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