RS886037963 NPRL2

Health Risk Chr 3:50350001
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What This Variant Does
"CLNSIG=5
Associated Conditions
Epilepsy
familial focal
with variable foci 2
Inborn genetic diseases
Seizure
Epilepsy
familial focal
with variable foci 2
Inborn genetic diseases
Seizure
Other Variants in NPRL2
rs2470932402 rs767088341 rs2109370013 rs2109365845 rs2470938044 rs147938650 rs139117542 rs1559857717 rs2470936665 rs2109368360
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