RS2088008490 DEPDC5

Health Risk Chr 22:31809628
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Associated Conditions
Inborn genetic diseases
Familial focal epilepsy with variable foci
Inborn genetic diseases
Familial focal epilepsy with variable foci
Other Variants in DEPDC5
rs768241563 rs587776973 rs587776974 rs587776975 rs879255234 rs587776976 rs587776977 rs587777458 rs587777459 rs541024038
Ask Dr. Hemsworth about this variant