List of variants reported as likely pathogenic for Rett syndrome, congenital variant by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_005249.5(FOXG1):c.573G>A (p.Met191Ile)	rs1555321311
NM_005249.5(FOXG1):c.578C>A (p.Ala193Asp)	rs2138661170
NM_005249.5(FOXG1):c.673T>G (p.Trp225Gly)
NM_005249.5(FOXG1):c.689G>T (p.Arg230Leu)	rs786205007
NM_005249.5(FOXG1):c.694A>G (p.Asn232Asp)	rs786205486
NM_005249.5(FOXG1):c.701C>T (p.Ser234Phe)	rs1555321334
NM_005249.5(FOXG1):c.703C>T (p.Leu235Phe)	rs1566445489
NM_005249.5(FOXG1):c.812G>A (p.Gly271Asp)	rs796052469

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