RS387907040 FA2H
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 35
Spastic paraplegia
Neurodegeneration with brain iron accumulation
Hereditary spastic paraplegia 35
Spastic paraplegia
Neurodegeneration with brain iron accumulation
Other Variants in FA2H