ClinVar Miner

List of variants studied for Rett syndrome, congenital variant by Fulgent Genetics, Fulgent Genetics

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Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_005249.5(FOXG1):c.1023C>G (p.Tyr341Ter) rs764343290
NM_005249.5(FOXG1):c.436_438del (p.Glu146del) rs751048593
NM_005249.5(FOXG1):c.460dup (p.Glu154fs) rs398124204

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