RS1057516161 FOXL2

Health Risk Chr 3:138946146
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What This Variant Does
"CLNSIG=5
Associated Conditions
Blepharophimosis
ptosis
and epicanthus inversus syndrome
Inborn genetic diseases
Blepharophimosis
ptosis
and epicanthus inversus syndrome
Inborn genetic diseases
Other Variants in FOXL2
rs104893741 rs387906321 rs863225450 rs863225451 rs863225452 rs797044528 rs797044532 rs104893737 rs104893738 rs387906322
Ask Dr. Hemsworth about this variant