List of variants reported as likely pathogenic for Rett syndrome, congenital variant by 3billion

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_005249.5(FOXG1):c.1020del (p.Tyr341fs)	rs2138661880
NM_005249.5(FOXG1):c.298C>T (p.Gln100Ter)
NM_005249.5(FOXG1):c.324_339dup (p.Ala114fs)	rs2138660628
NM_005249.5(FOXG1):c.568A>T (p.Ile190Phe)
NM_005249.5(FOXG1):c.620T>C (p.Ile207Thr)	rs1881803464
NM_005249.5(FOXG1):c.844dup (p.Ala282fs)	rs2138661638

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