List of variants in gene FOXC1 reported as likely pathogenic for Congenital anomaly of kidney and urinary tract

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001453.3(FOXC1):c.1090C>T (p.Pro364Ser)	rs867806300	0.00001
NM_001453.3(FOXC1):c.176G>T (p.Gly59Val)	rs1762519001	0.00001
NM_001453.3(FOXC1):c.1025C>T (p.Ala342Val)	rs773600190
NM_001453.3(FOXC1):c.1139G>T (p.Gly380Val)	rs1581374640
NM_001453.3(FOXC1):c.207GCAGCC[3] (p.70QP[3])	rs780038931
NM_001453.3(FOXC1):c.430AAG[1] (p.Lys145del)	rs768741176
NM_001453.3(FOXC1):c.926_940del (p.Ser309_Ile313del)	rs774848608

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