ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.689G>A (p.Arg230His)

dbSNP: rs786205007
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
RettBASE RCV000170080 SCV000222393 pathogenic Rett syndrome, congenital variant 2013-02-15 no assertion criteria provided curation

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