RS878854991 SPAST
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 4
Inborn genetic diseases
Abnormal central motor function
Hereditary spastic paraplegia
SPAST-related disorder
Hereditary spastic paraplegia 4
Hereditary spastic paraplegia 4
Inborn genetic diseases
Abnormal central motor function
Hereditary spastic paraplegia
SPAST-related disorder
Hereditary spastic paraplegia 4
Other Variants in SPAST