ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.1433-6C>A

dbSNP: rs747745989
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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 RCV001227740 SCV001400110 likely benign Birt-Hogg-Dube syndrome 2023-04-22 criteria provided, single submitter clinical testing

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