RS151104648 LGI1

Health Risk Chr 10:93777436
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Associated Conditions
Epilepsy
familial temporal lobe
1
Autosomal dominant epilepsy with auditory features
Inborn genetic diseases
Epilepsy
familial temporal lobe
1
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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