RS2536301748 CNTNAP2

Health Risk Chr 7:147903567
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Associated Conditions
Inborn genetic diseases
Cortical dysplasia-focal epilepsy syndrome
Inborn genetic diseases
Cortical dysplasia-focal epilepsy syndrome
Other Variants in CNTNAP2
rs730880275 rs2710102 rs7794745 rs121908445 rs730880276 rs267601384 rs139180845 rs143877693 rs398124268 rs145162968
Ask Dr. Hemsworth about this variant