ClinVar Miner

Submissions for variant NM_001453.3(FOXC1):c.1025C>G (p.Ala342Gly)

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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 RCV002644216 SCV003522343 likely benign Axenfeld-Rieger syndrome type 3 2022-04-08 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003434592 SCV004158206 uncertain significance not provided 2023-01-01 criteria provided, single submitter clinical testing

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