RS781404129 LGI1

Health Risk Chr 10:93793250
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Associated Conditions
Autosomal dominant epilepsy with auditory features
Inborn genetic diseases
Autosomal dominant epilepsy with auditory features
Inborn genetic diseases
Other Variants in LGI1
rs28937874 rs2134020917 rs1589762127 rs104894166 rs28939075 rs2134001459 rs104894167 rs119488099 rs119488100 rs587780379
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