RS312262752 SPG11
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 11
Amyotrophic lateral sclerosis type 5
SPG11-related disorder
Charcot-Marie-Tooth disease axonal type 2X
Hereditary spastic paraplegia 11
Amyotrophic lateral sclerosis type 5
SPG11-related disorder
Charcot-Marie-Tooth disease axonal type 2X
Other Variants in SPG11