RS587776975 DEPDC5

Health Risk Chr 22:31893655
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Epilepsy
familial focal
with variable foci 1
Autosomal dominant epilepsy
Epilepsy
familial focal
with variable foci 1
Autosomal dominant epilepsy
Other Variants in DEPDC5
rs768241563 rs587776973 rs587776974 rs879255234 rs587776976 rs587776977 rs587777458 rs587777459 rs541024038 rs564667614
Ask Dr. Hemsworth about this variant