List of variants in gene FOXC1 reported as benign by Eurofins NTD LLC (GA)

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: 9

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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.502C>T (p.Leu168=)	rs148739656	0.00363
NM_001453.3(FOXC1):c.921C>T (p.Gly307=)	rs369300819	0.00105
NM_001453.3(FOXC1):c.1124GCG[7] (p.Gly380dup)	rs76840944
NM_001453.3(FOXC1):c.1142_1144dup (p.Ala381dup)	rs796065323
NM_001453.3(FOXC1):c.1338CGG[7] (p.Gly456del)	rs398123612
NM_001453.3(FOXC1):c.1338CGG[9] (p.Gly456dup)	rs398123612

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