ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.443G>C (p.Gly148Ala)

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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 RCV003104389 SCV003780833 benign Rett syndrome, congenital variant 2023-08-04 criteria provided, single submitter clinical testing

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