ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.498G>C (p.Gly166=)

dbSNP: rs764054659
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000194604 SCV000247417 uncertain significance not specified 2014-12-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002056987 SCV002351944 likely benign Rett syndrome, congenital variant 2022-05-04 criteria provided, single submitter clinical testing

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