RS202148793 LGI1

Health Risk Chr 10:93797284
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Associated Conditions
Epilepsy
familial temporal lobe
1
Inborn genetic diseases
Autosomal dominant epilepsy with auditory features
Epilepsy
familial temporal lobe
1
Inborn genetic diseases
Autosomal dominant epilepsy with auditory features
Other Variants in LGI1
rs28937874 rs2134020917 rs1589762127 rs104894166 rs28939075 rs2134001459 rs104894167 rs119488099 rs119488100 rs587780379
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