ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.871+13T>C

dbSNP: rs770537219
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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 RCV002142399 SCV002411839 likely benign Birt-Hogg-Dube syndrome 2024-01-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002508031 SCV002809234 likely benign Birt-Hogg-Dube syndrome; Familial spontaneous pneumothorax; Potocki-Lupski syndrome; Nonpapillary renal cell carcinoma; Colorectal cancer 2022-03-28 criteria provided, single submitter clinical testing

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