ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.765G>T (p.Trp255Cys)

dbSNP: rs121913678
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000145997 SCV000193146 pathogenic Rett syndrome, congenital variant 2015-05-04 criteria provided, single submitter clinical testing

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