ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.618C>T (p.Gly206=)

gnomAD frequency: 0.00001  dbSNP: rs930327703
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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 RCV000871578 SCV001013255 likely benign Rett syndrome, congenital variant 2023-04-06 criteria provided, single submitter clinical testing

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