ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.150C>T (p.His50=)

gnomAD frequency: 0.00001  dbSNP: rs532508999
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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 RCV001409853 SCV001611887 likely benign Rett syndrome, congenital variant 2023-08-10 criteria provided, single submitter clinical testing
GeneDx RCV001546304 SCV001765800 likely benign not provided 2020-01-06 criteria provided, single submitter clinical testing

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