ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.132G>A (p.Gln44=)

dbSNP: rs2145045741
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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 RCV002089897 SCV002325068 likely benign Birt-Hogg-Dube syndrome 2024-02-10 criteria provided, single submitter clinical testing

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