RS1064794249 LGI1

Health Risk Chr 10:93797550
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal dominant epilepsy with auditory features
Autosomal dominant epilepsy with auditory features
Other Variants in LGI1
rs28937874 rs2134020917 rs1589762127 rs104894166 rs28939075 rs2134001459 rs104894167 rs119488099 rs119488100 rs587780379
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