RS147938650 NPRL2

Health Risk Chr 3:50348403
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Associated Conditions
Epilepsy
familial focal
with variable foci 2
Inborn genetic diseases
Epilepsy
familial focal
with variable foci 2
Inborn genetic diseases
Other Variants in NPRL2
rs2470932402 rs2109368360 rs767088341 rs2109370013 rs2109365845 rs2470938044 rs139117542 rs1559857717 rs2470936665 rs2109364484
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