List of variants in gene FOXC2 reported as uncertain significance for immune system disorder

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_005251.3(FOXC2):c.1331A>G (p.Gln444Arg)	rs147258453	0.00136
NM_005251.3(FOXC2):c.1169_1189del (p.Gln390_His396del)	rs976840192
NM_005251.3(FOXC2):c.1265C>T (p.Ala422Val)
NM_005251.3(FOXC2):c.390C>A (p.Phe130Leu)
NM_005251.3(FOXC2):c.529_531del (p.Lys177del)
NM_005251.3(FOXC2):c.760G>C (p.Gly254Arg)	rs966178183
NM_005251.3(FOXC2):c.782C>A (p.Ala261Asp)	rs1974225710
NM_005251.3(FOXC2):c.889GTG[3] (p.Val298dup)	rs758855849

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