RS1057519479 FOXC1

Health Risk Chr 6:1611110
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What This Variant Does
"CLNSIG=5
Associated Conditions
Axenfeld-Rieger syndrome type 3
Hypertelorism and tetralogy of fallot
Axenfeld-Rieger syndrome type 3
Hypertelorism and tetralogy of fallot
Other Variants in FOXC1
rs2113111009 rs104893957 rs104893958 rs104893951 rs104893952 rs104893953 rs104893954 rs121909338 rs121909339 rs372857241
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