ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.209AGC[2] (p.Gln72_Gln73del)

dbSNP: rs398124201
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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 RCV001403288 SCV001605154 likely benign Rett syndrome, congenital variant 2020-08-14 criteria provided, single submitter clinical testing

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