ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.447C>G (p.Ala149=)

dbSNP: rs112803404
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001580781 SCV001817812 likely benign not provided 2020-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003771783 SCV004661727 likely benign Rett syndrome, congenital variant 2024-01-19 criteria provided, single submitter clinical testing

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