ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.318G>A (p.Pro106=)

gnomAD frequency: 0.00001  dbSNP: rs1035987967
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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 RCV001468358 SCV001672402 likely benign Rett syndrome, congenital variant 2023-09-12 criteria provided, single submitter clinical testing
GeneDx RCV001581148 SCV001819886 likely benign not provided 2019-10-07 criteria provided, single submitter clinical testing

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