RS137906617 CLN3

Health Risk Chr 16:28488643
Upload your DNA to see your genotype for this variant.
Associated Conditions
Progressive myoclonic epilepsy type 3
Neuronal ceroid lipofuscinosis
Neuronal ceroid lipofuscinosis 3
Inborn genetic diseases
Progressive myoclonic epilepsy type 3
Neuronal ceroid lipofuscinosis
Neuronal ceroid lipofuscinosis 3
Inborn genetic diseases
Other Variants in CLN3
rs1555468634 rs121434286 rs267606737 rs386833694 rs386833695 rs386833696 rs386833697 rs386833698 rs386833699 rs386833700
Ask Dr. Hemsworth about this variant