RS312262770 SPG11

Health Risk Chr 15:44583911
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 11
Inborn genetic diseases
Hereditary spastic paraplegia
Charcot-Marie-Tooth disease axonal type 2X
Hereditary spastic paraplegia 11
Inborn genetic diseases
Hereditary spastic paraplegia
Charcot-Marie-Tooth disease axonal type 2X
Other Variants in SPG11
rs118203963 rs312262716 rs267607084 rs312262720 rs312262744 rs312262715 rs200079802 rs141848292 rs312262752 rs312262722
Ask Dr. Hemsworth about this variant