List of variants reported as likely pathogenic for Greig cephalopolysyndactyly syndrome

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000168.6(GLI3):c.539G>A (p.Arg180Gln)	rs140772904	0.00009
NM_000168.6(GLI3):c.1459T>A (p.Cys487Ser)
NM_000168.6(GLI3):c.1873C>T (p.Arg625Trp)	rs121917712
NM_000168.6(GLI3):c.2686G>C (p.Asp896His)
NM_000168.6(GLI3):c.4076G>A (p.Gly1359Glu)	rs1583728402
NM_000168.6(GLI3):c.4445del (p.Pro1482fs)
NM_000168.6(GLI3):c.793del (p.Ala265fs)	rs2128741200

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