RS1057521725 RBFOX1

Health Risk Chr 16:7579859
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What This Variant Does
"CLNSIG=4
Associated Conditions
Idiopathic generalized epilepsy
Inborn genetic diseases
Intellectual disability
autosomal dominant 46
Neurodevelopmental disorder
Idiopathic generalized epilepsy
Inborn genetic diseases
Intellectual disability
autosomal dominant 46
Neurodevelopmental disorder
Other Variants in RBFOX1
rs1064794750 rs139251660 rs147306562 rs145351963 rs2093621567 rs141919506 rs376061440 rs2510618048 rs2509828295
Ask Dr. Hemsworth about this variant