RS749199519 PRKCG

Health Risk Chr 19:53900703
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Autosomal dominant cerebellar ataxia
Inborn genetic diseases
Autosomal dominant cerebellar ataxia
Other Variants in PRKCG
rs121918511 rs121918512 rs121918513 rs121918514 rs121918515 rs121918516 rs121918517 rs121918518 rs1555808841 rs387906679
Ask Dr. Hemsworth about this variant