List of variants in gene FOXF1 reported as benign for congenital anomaly of cardiovascular system

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001451.3(FOXF1):c.645C>T (p.His215=)	rs61740819	0.02277
NM_001451.3(FOXF1):c.873C>T (p.Ser291=)	rs61753347	0.01583
NM_001451.3(FOXF1):c.1083G>A (p.Gly361=)	rs112197095	0.00477
NM_001451.3(FOXF1):c.908G>A (p.Ser303Asn)	rs200676463	0.00467
NM_001451.3(FOXF1):c.1175_1176del	rs397854726
NM_001451.3(FOXF1):c.*1176del	rs397854726
NM_001451.3(FOXF1):c.*472dup	rs56130003

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