ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.183_206del (p.Ala62_Pro69del) (rs587783632)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory,University of Chicago RCV000145984 SCV000193133 likely benign not specified 2013-02-08 criteria provided, single submitter clinical testing
GeneDx RCV000145984 SCV000241021 likely benign not specified 2012-05-14 criteria provided, single submitter clinical testing The variant is found in EPILEPSY panel(s).
Invitae RCV000808453 SCV000948562 likely benign Rett syndrome, congenital variant 2019-10-24 criteria provided, single submitter clinical testing

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