ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.803G>T (p.Gly268Val)

dbSNP: rs2138661568
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002114366 SCV002447600 likely benign Rett syndrome, congenital variant 2022-08-09 criteria provided, single submitter clinical testing

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