RS767350733 ALS2

Health Risk Chr 2:201724392
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Amyotrophic lateral sclerosis type 2
juvenile
Infantile-onset ascending hereditary spastic paralysis
Juvenile primary lateral sclerosis
Inborn genetic diseases
Amyotrophic lateral sclerosis type 2
juvenile
Infantile-onset ascending hereditary spastic paralysis
Juvenile primary lateral sclerosis
Other Variants in ALS2
rs386134173 rs386134181 rs386134176 rs386134187 rs387906316 rs386134183 rs386134175 rs386134188 rs121908137 rs386134174
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