RS312262722 SPG11

Health Risk Chr 15:44651744
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 11
Inborn genetic diseases
SPG11-related disorder
Amyotrophic lateral sclerosis type 5
Charcot-Marie-Tooth disease axonal type 2X
See cases
Hereditary spastic paraplegia 11
Inborn genetic diseases
SPG11-related disorder
Amyotrophic lateral sclerosis type 5
Charcot-Marie-Tooth disease axonal type 2X
See cases
Other Variants in SPG11
rs118203963 rs312262716 rs267607084 rs312262720 rs312262744 rs312262715 rs200079802 rs141848292 rs312262752 rs312262723
Ask Dr. Hemsworth about this variant