List of variants in gene FOXF1 reported as uncertain significance for congenital pulmonary veins anomaly

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001451.3(FOXF1):c.309_310insT	rs11392376	0.46626
NM_001451.3(FOXF1):c.636G>C (p.Ser212=)	rs776649998	0.00001
NM_001451.3(FOXF1):c.*1176del	rs397854726
NM_001451.3(FOXF1):c.*123dup	rs886052379
NM_001451.3(FOXF1):c.*1298dup	rs886052386
NM_001451.3(FOXF1):c.310_311insT	rs67178865
NM_001451.3(FOXF1):c.471_472dup	rs56130003
NM_001451.3(FOXF1):c.-2C>T	rs1969543882
NM_001451.3(FOXF1):c.1070A>T (p.His357Leu)
NM_001451.3(FOXF1):c.166C>T (p.Leu56Phe)
NM_001451.3(FOXF1):c.47_48insGCGGCGGCGGCGGGGGAG (p.Gly16_Gly17insArgArgArgArgGlySer)
NM_001451.3(FOXF1):c.602G>A (p.Gly201Asp)
NM_001451.3(FOXF1):c.60_62del (p.Gly23del)	rs757668134
NM_001451.3(FOXF1):c.771G>T (p.Met257Ile)
NM_001451.3(FOXF1):c.881_902dup (p.Gly302fs)

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