RS113994068 EIF2B5
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Vanishing white matter disease
Leukoencephalopathy with vanishing white matter 5
Inborn genetic diseases
Vanishing white matter disease
Leukoencephalopathy with vanishing white matter 5
Inborn genetic diseases
Other Variants in EIF2B5