ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.1488T>C (p.Ser496=)

dbSNP: rs2046868610
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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 RCV001445882 SCV001648921 likely benign Birt-Hogg-Dube syndrome 2019-06-27 criteria provided, single submitter clinical testing

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