ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.1062+8G>A

dbSNP: rs1317761101
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001393251 SCV001594911 likely benign Birt-Hogg-Dube syndrome 2021-06-05 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005245844 SCV005899753 likely benign Birt-Hogg-Dube syndrome 1 2024-10-24 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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