RS752550849 CNTNAP2

Health Risk Chr 7:147300239
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cortical dysplasia-focal epilepsy syndrome
See cases
Inborn genetic diseases
Cortical dysplasia-focal epilepsy syndrome
See cases
Inborn genetic diseases
Other Variants in CNTNAP2
rs730880275 rs2710102 rs7794745 rs121908445 rs730880276 rs267601384 rs139180845 rs143877693 rs398124268 rs145162968
Ask Dr. Hemsworth about this variant