ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.*3C>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV005246279 SCV005896581 benign Birt-Hogg-Dube syndrome 1 2024-10-28 criteria provided, single submitter clinical testing This variant is considered benign. This variant occurs in the non-coding 3' untranslated region of the gene, and is not expected to impact protein function.

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