RS119488099 LGI1

Health Risk Chr 10:93777592
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What This Variant Does
"[OMIM:?]
Associated Conditions
Epilepsy
familial temporal lobe
1
Autosomal dominant epilepsy with auditory features
LGI1-related disorder
Epilepsy
familial temporal lobe
1
Autosomal dominant epilepsy with auditory features
LGI1-related disorder
Other Variants in LGI1
rs28937874 rs2134020917 rs1589762127 rs104894166 rs28939075 rs2134001459 rs104894167 rs119488100 rs587780379 rs151104648
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