ClinVar Miner

List of variants reported as uncertain significance for Rett syndrome, congenital variant by Center for Human Genetics, Inc, Center for Human Genetics, Inc

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005249.5(FOXG1):c.218A>C (p.Gln73Pro)	rs760663911	0.00015
NM_005249.5(FOXG1):c.460GAG[1] (p.Glu155del)	rs1175471807
NM_005249.5(FOXG1):c.565C>G (p.Leu189Val)	rs1555321308

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