RS104893859 PITX2

Health Risk Chr 4:110618669
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What This Variant Does
"[OMIM:?]
Associated Conditions
Axenfeld-Rieger syndrome type 1
Inborn genetic diseases
Axenfeld-Rieger syndrome type 1
Anterior segment dysgenesis 4
Axenfeld-Rieger syndrome type 1
Inborn genetic diseases
Axenfeld-Rieger syndrome type 1
Anterior segment dysgenesis 4
Other Variants in PITX2
rs104893857 rs1560590094 rs104893858 rs1198152064 rs104893860 rs121909248 rs104893861 rs1553922583 rs121909249 rs2529773041
Ask Dr. Hemsworth about this variant