RS312262749 SPG11

Health Risk Chr 15:44620189
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 11
Amyotrophic lateral sclerosis type 5
Charcot-Marie-Tooth disease axonal type 2X
Inborn genetic diseases
Hereditary spastic paraplegia 11
Hereditary spastic paraplegia 11
Amyotrophic lateral sclerosis type 5
Charcot-Marie-Tooth disease axonal type 2X
Inborn genetic diseases
Hereditary spastic paraplegia 11
Other Variants in SPG11
rs118203963 rs312262716 rs267607084 rs312262720 rs312262744 rs312262715 rs200079802 rs141848292 rs312262752 rs312262722
Ask Dr. Hemsworth about this variant