ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.1300+13G>A

gnomAD frequency: 0.00004  dbSNP: rs754300911
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002083892 SCV002378742 likely benign Birt-Hogg-Dube syndrome 2025-02-03 criteria provided, single submitter clinical testing

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