RS878853157 PDE8B

Health Risk Chr 5:77211001
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant striatal neurodegeneration type 1
Autosomal dominant striatal neurodegeneration type 1
Other Variants in PDE8B
rs374692260 rs1389677367 rs2531241138 rs561890042 rs2531989713 rs1793090227 rs2149371468 rs2149371436 rs1796729286 rs121918360
Ask Dr. Hemsworth about this variant