RS863223696 MED12

Health Risk Chr X:71132100
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What This Variant Does
"CLNSIG=5
Associated Conditions
FG syndrome 1
Inborn genetic diseases
Blepharophimosis - intellectual disability syndrome
MKB type
FG syndrome
FG syndrome 1
Inborn genetic diseases
Blepharophimosis - intellectual disability syndrome
MKB type
FG syndrome
Other Variants in MED12
rs80338758 rs80338759 rs387907360 rs387907361 rs387907362 rs398124196 rs398124197 rs56658066 rs398124198 rs398124199
Ask Dr. Hemsworth about this variant