List of variants reported as uncertain significance for GATA6-related congenital heart disease with or without pancreatic agenesis or neonatal diabetes by Fulgent Genetics, Fulgent Genetics

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_005257.6(GATA6):c.839G>C (p.Gly280Ala)	rs904519303	0.00022
NM_005257.6(GATA6):c.1027G>A (p.Ala343Thr)	rs142601402	0.00016
NM_005257.6(GATA6):c.551G>A (p.Ser184Asn)	rs387906816	0.00014
NM_005257.6(GATA6):c.259C>T (p.Pro87Ser)	rs563978220	0.00010
NM_005257.6(GATA6):c.660C>T (p.Gly220=)	rs1385756157	0.00006
NM_005257.6(GATA6):c.367A>G (p.Thr123Ala)	rs1194141406	0.00002
NM_005257.6(GATA6):c.233T>C (p.Leu78Pro)	rs1253034411
NM_005257.6(GATA6):c.37C>T (p.Arg13Cys)

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