List of variants in gene FOXC1 reported as pathogenic for anterior segment dysgenesis 3

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001453.3(FOXC1):c.889C>T (p.Pro297Ser)	rs79691946	0.03108
FOXC1, 22-BP INS, NT26
FOXC1, DUP
NM_001453.3(FOXC1):c.153_163del (p.His52fs)	rs2113111009
NM_001453.3(FOXC1):c.349del (p.Asp117fs)	rs1554100953
NM_001453.3(FOXC1):c.378C>G (p.Ile126Met)	rs104893958
NM_001453.3(FOXC1):c.392C>T (p.Ser131Leu)	rs104893957
NM_001453.3(FOXC1):c.398_401del (p.Asn133fs)	rs2113111662
NM_001453.3(FOXC1):c.487G>T (p.Glu163Ter)	rs1057519477
NM_001453.3(FOXC1):c.718_719del (p.Leu240fs)	rs1057519480

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