ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.963C>T (p.Ala321=)

gnomAD frequency: 0.00001  dbSNP: rs781085552
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001469055 SCV001673127 likely benign Rett syndrome, congenital variant 2021-11-03 criteria provided, single submitter clinical testing

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