RS104893957 FOXC1

Health Risk Chr 6:1610837
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What This Variant Does
"[OMIM:?]
Associated Conditions
Anterior segment dysgenesis 3
Axenfeld-Rieger syndrome type 3
Inborn genetic diseases
Axenfeld-Rieger syndrome type 3
Anterior segment dysgenesis 3
Axenfeld-Rieger syndrome type 3
Inborn genetic diseases
Axenfeld-Rieger syndrome type 3
Other Variants in FOXC1
rs2113111009 rs104893958 rs104893951 rs104893952 rs104893953 rs104893954 rs121909338 rs121909339 rs372857241 rs483352810
Ask Dr. Hemsworth about this variant