RS113994049 EIF2B5
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What This Variant Does
"[OMIM:?]
Associated Conditions
Vanishing white matter disease
See cases
Leukoencephalopathy with vanishing white matter 5
Inborn genetic diseases
EIF2B5-related disorder
Vanishing white matter disease
See cases
Leukoencephalopathy with vanishing white matter 5
Inborn genetic diseases
EIF2B5-related disorder
Other Variants in EIF2B5