List of variants in gene FOXC1 reported as benign by GeneDx

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001453.3(FOXC1):c.1563T>G (p.Ser521=)	rs73406891	0.03175
NM_001453.3(FOXC1):c.889C>T (p.Pro297Ser)	rs79691946	0.03108
NM_001453.3(FOXC1):c.405C>T (p.Cys135=)	rs2230096	0.03096
NM_001453.3(FOXC1):c.*52G>A	rs73406893	0.02925
NM_001453.3(FOXC1):c.1211C>T (p.Ala404Val)	rs865901577	0.00024
NM_001453.3(FOXC1):c.*105C>A	rs116336796
NM_001453.3(FOXC1):c.1124GCG[7] (p.Gly380dup)	rs76840944
NM_001453.3(FOXC1):c.1124_1125insGCG (p.Gly375_Gly376insArg)	rs2113113713
NM_001453.3(FOXC1):c.1139_1140insGCG (p.Gly380_Ala381insArg)	rs2113113820
NM_001453.3(FOXC1):c.1338_1339insCGG (p.His446_Gly447insArg)	rs373075286
NM_001453.3(FOXC1):c.1359_1360insCGG (p.Gly453_Gly454insArg)	rs2113114648
NM_001453.3(FOXC1):c.83CGGCGGCCG[1] (p.Ala31_Ala33del)	rs756196843

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