RS377536938 PDE8B

Health Risk Chr 5:77329000
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Associated Conditions
Autosomal dominant striatal neurodegeneration type 1
Inborn genetic diseases
Autosomal dominant striatal neurodegeneration type 1
Inborn genetic diseases
Other Variants in PDE8B
rs374692260 rs1389677367 rs2531241138 rs561890042 rs2531989713 rs1793090227 rs2149371468 rs2149371436 rs1796729286 rs121918360
Ask Dr. Hemsworth about this variant