ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.655C>G (p.Arg219Gly)

dbSNP: rs1555321323
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
NeuroMeGen, Hospital Clinico Santiago de Compostela RCV000585867 SCV000693801 uncertain significance Rett syndrome, congenital variant 2018-01-01 criteria provided, single submitter clinical testing

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