ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.1176+17C>G

dbSNP: rs376932013
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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 RCV002104759 SCV002389179 likely benign Birt-Hogg-Dube syndrome 2021-10-07 criteria provided, single submitter clinical testing

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