RS143877693 CNTNAP2

Health Risk Chr 7:147132381
Upload your DNA to see your genotype for this variant.
Associated Conditions
Cortical dysplasia-focal epilepsy syndrome
Inborn genetic diseases
CNTNAP2-related disorder
Cortical dysplasia-focal epilepsy syndrome
Inborn genetic diseases
CNTNAP2-related disorder
Other Variants in CNTNAP2
rs730880275 rs2710102 rs7794745 rs121908445 rs730880276 rs267601384 rs139180845 rs398124268 rs145162968 rs375318010
Ask Dr. Hemsworth about this variant