ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.1219G>C (p.Val407Leu)

dbSNP: rs1287203413
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Génétique des Maladies du Développement, Hospices Civils de Lyon RCV001290335 SCV001478269 benign Rett syndrome, congenital variant criteria provided, single submitter clinical testing

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