ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.931_932dup (p.Val312fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute for Human Genetics and Genomic Medicine, Uniklinik RWTH Aachen RCV002308476 SCV002586995 likely pathogenic Birt-Hogg-Dube syndrome 2022-10-26 criteria provided, single submitter clinical testing

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