ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.505_506delinsC (p.Gly169fs)

dbSNP: rs786205003
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000502824 SCV000594862 pathogenic FOXG1 disorder 2016-01-04 criteria provided, single submitter clinical testing

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