RS312262755 SPG11

Health Risk Chr 15:44600488
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 11
Spastic paraplegia
Inborn genetic diseases
Hereditary neuropathy or pain disorder
Hereditary spastic paraplegia 11
Spastic paraplegia
Inborn genetic diseases
Hereditary neuropathy or pain disorder
Other Variants in SPG11
rs118203963 rs312262716 rs267607084 rs312262720 rs312262744 rs312262715 rs200079802 rs141848292 rs312262752 rs312262722
Ask Dr. Hemsworth about this variant