RS397518459 SPAG1

Health Risk Chr 8:100184711
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant nocturnal frontal lobe epilepsy 5
Autosomal dominant nocturnal frontal lobe epilepsy 5
Other Variants in SPAG1
rs397518458 rs201740530 rs886037653 rs149271265 rs878855237 rs142031266 rs1060503107 rs752479330 rs544372581 rs1060503104
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