RS797044934 ALS2

Health Risk Chr 2:201704160
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Infantile-onset ascending hereditary spastic paralysis
Inborn genetic diseases
Infantile-onset ascending hereditary spastic paralysis
Other Variants in ALS2
rs386134173 rs386134181 rs386134176 rs386134187 rs387906316 rs386134183 rs386134175 rs386134188 rs121908137 rs386134174
Ask Dr. Hemsworth about this variant