RS564667614 DEPDC5

Health Risk Chr 22:31843170
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What This Variant Does
"CLNSIG=255
Associated Conditions
Epilepsy
familial focal
with variable foci 1
Familial focal epilepsy with variable foci
Inborn genetic diseases
Autosomal dominant nocturnal frontal lobe epilepsy
Epilepsy
familial focal
with variable foci 1
Familial focal epilepsy with variable foci
Inborn genetic diseases
Autosomal dominant nocturnal frontal lobe epilepsy
Other Variants in DEPDC5
rs768241563 rs587776973 rs587776974 rs587776975 rs879255234 rs587776976 rs587776977 rs587777458 rs587777459 rs541024038
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